Methods of making organic compounds by metathesis

ABSTRACT

Described are methods of making organic compounds by metathesis chemistry. The methods of the invention are particularly useful for making industrially-important organic compounds beginning with starting compositions derived from renewable feedstocks, such as natural oils. The methods make use of a cross-metathesis step with an olefin compound to produce functionalized alkene intermediates having a pre-determined double bond position. Once isolated, the functionalized alkene intermediate can be self-metathesized or cross-metathesized (e.g., with a second functionalized alkene) to produce the desired organic compound or a precursor thereto. The method may be used to make bifunctional organic compounds, such as diacids, diesters, dicarboxylate salts, acid/esters, acid/amines, acid/alcohols, acid/aldehydes, acid/ketones, acid/halides, acid/nitriles, ester/amines, ester/alcohols, ester/aldehydes, ester/ketones, ester/halides, ester/nitriles, and the like.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation-in-part of International Application No. PCT/US2007/021933, filed Oct. 15, 2007, which claims the benefit of U.S. Provisional Application having Ser. No. 60/851,632, filed Oct. 13, 2006, and entitled METHODS OF MAKING ORGANIC COMPOUNDS BY METATHESIS, the disclosures of which are incorporated herein by reference.

GOVERNMENT RIGHTS

This invention was made with U.S. Government support under Award Number DE-FG36-04GO14016 awarded by the U.S. Department of Energy. The Government may have certain rights in this invention.

BACKGROUND

It is desirable to use renewable feedstocks (e.g., natural oil-derived fatty acids or fatty esters) as a source material for synthesizing industrially important organic compounds that have been conventionally manufactured from petroleum feedstocks. One useful reaction for modifying the structure of natural oil-derived feedstocks is metathesis. Metathesis is a catalytic reaction involving the rupture and reformation of carbon-carbon double bonds. When metathesis is applied directly to many natural oil-derived feedstocks, a mixture of products results. For example, when metathesis is applied to a mixture of fatty acid esters, the resulting metathesis products include a mixture of monoesters and diesters of various chain lengths. Due to the similarity in molecular weight and functionality of the products, it is difficult to separate the desired product (e.g., a particular chain length diester) from the other metathesis products.

In view of the foregoing, what is desired is a method by which bifunctional compounds such as dicarboxylic acids, dicarboxylate esters, and dicarboxylate salt compounds can be manufactured in high yields from metathesis reactions applied to starting materials such as fatty acids, fatty esters, fatty acid salts, and mixtures thereof.

SUMMARY

The invention relates to methods of making organic compounds by metathesis chemistry. The methods of the invention are particularly useful for making industrially-important organic compounds from starting compositions that are derived from renewable feedstocks, such as natural oils.

The methods of the invention make use of a cross-metathesis step with an olefin compound to produce functionalized alkene intermediates having a pre-determined double bond position. Advantageously, the functionalized alkene intermediates can be isolated at high purity from the other cross-metathesis products and from any remaining starting material. Once isolated, the functionalized alkene intermediate can be self-metathesized or cross-metathesized (e.g., with a second functionalized alkene) to produce the desired bifunctional organic compound or a precursor thereto. Representative organic compounds include bifunctional organic compounds, such as diacids, diesters, dicarboxylate salts, acid/esters, acid/amines, acid/alcohols, acid/aldehydes, acid/ketones, acid/halides, acid/nitriles, ester/amines, ester/alcohols, ester/aldehydes, ester/ketones, ester/halides, ester/nitriles, and the like.

Accordingly, in one aspect, the invention provides a method of making diacid alkenes, diester alkenes, or dicarboxylate salt alkenes by metathesis. The method of the invention comprises the steps of:

(a) providing a starting composition comprising one or more unsaturated fatty acids, unsaturated fatty esters, or unsaturated fatty acid salts;

(b) cross-metathesizing the composition of step (a) with a short-chain olefin in the presence of a first metathesis catalyst, to form cross-metathesis products comprising: (i) one or more olefins; and (ii) one or more acid-, ester-, or carboxylate salt-functionalized alkenes;

(c) separating at least a portion of one or more of the acid-, ester-, or carboxylate salt-functionalized alkenes from the cross-metathesis products; and

(d) self-metathesizing the separated acid-, ester-, or carboxylate salt-functionalized alkene in the presence of a second metathesis catalyst to form a composition comprising one or more diacid alkenes, diester alkenes, or dicarboxylate salt alkenes.

In another aspect, the invention provides a method of making bifunctional organic compounds, the method comprising the steps of:

(a) providing a starting composition comprising one or more unsaturated fatty acids, unsaturated fatty esters, or unsaturated fatty acid salts;

(b) cross-metathesizing the starting composition of step (a) with a short-chain olefin in the presence of a first metathesis catalyst to form cross-metathesis products comprising: (i) one or more olefins; and (ii) one or more acid-, ester-, or carboxylate salt-functionalized alkenes;

(c) separating at least a portion of the one or more acid-, ester-, or carboxylate salt-functionalized alkenes from the cross-metathesis products; and

(d) cross-metathesizing the separated acid-, ester-, or carboxylate salt-functionalized alkenes with a second functionalized alkene in the presence of a metathesis catalyst to form a composition comprising a bifunctional organic compound.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a process flow diagram of an embodiment of the method of the invention.

FIG. 2 is a process flow diagram of an embodiment of the method of the invention.

FIG. 2A is a process flow diagram of an embodiment of the method of the invention.

FIG. 2B is a process flow diagram of an embodiment of the method of the invention.

FIG. 3 is a process flow diagram of an embodiment of the method of the invention.

DETAILED DESCRIPTION Starting Composition (Step (a))

As a starting composition, the method of the present invention uses unsaturated fatty acids, unsaturated fatty esters, salts of unsaturated fatty acids, or a mixture. As used herein the term “unsaturated fatty acid” refers to compounds that have an alkene chain with a terminal carboxylic acid group. The alkene chain may be a linear or branched and may optionally include one or more functional groups in addition to the carboxylic acid group. For example, some carboxylic acids include one or more hydroxyl groups. The alkene chain typically contains about 4 to about 30 carbon atoms, more typically about 4 to about 22 carbon atoms. In many embodiments, the alkene chain contains 18 carbon atoms (i.e., a C18 fatty acid). The unsaturated fatty acids have at least one carbon-carbon double bond in the alkene chain (i.e., a monounsaturated fatty acid), and may have more than one double bond (i.e., a polyunsaturated fatty acid) in the alkene chain. In exemplary embodiments, the unsaturated fatty acid has from 1 to 3 carbon-carbon double bonds in the alkene chain.

Also useful as starting compositions are unsaturated fatty esters. As used herein the term “unsaturated fatty ester” refers to a compounds that have an alkene chain with a terminal ester group. The alkene chain may be linear or branched and may optionally include one or more functional groups in addition to the ester group. For example, some unsaturated fatty esters include one or more hydroxyl groups in addition to the ester group. Unsaturated fatty esters include “unsaturated monoesters” and “unsaturated polyol esters”. Unsaturated monoesters have an alkene chain that terminates in an ester group, for example, an alkyl ester group such as a methyl ester. The alkene chain of the unsaturated monoesters typically contains about 4 to about 30 carbon atoms, more typically about 4 to 22 carbon atoms. In exemplary embodiments, the alkene chain contains 18 carbon atoms (i.e., a C18 fatty ester). The unsaturated monoesters have at least one carbon-carbon double bond in the alkene chain and may have more than one double bond in the alkene chain. In exemplary embodiments, the unsaturated fatty ester has 1 to 3 carbon-carbon double bonds in the alkene chain.

Also useful as a starting composition are metal salts of unsaturated fatty acids (i.e., carboxylate salts of unsaturated fatty acids). The metal salts may be salts of alkali metals (e.g., a group IA metal such as Li, Na, K, Rb, and Cs); alkaline earth metals (e.g., group IIA metals such as Be, Mg, Ca, Sr, and Ba); group IIIA metals (e.g., B, Al, Ga, In, and Tl); group IVA metals (e.g., Sn and Pb), group VA metals (e.g., Sb and Bi), transition metals (e.g., Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Zr, Mo, Ru, Rh, Pd, Ag and Cd), lanthanides or actinides.

In many embodiments, the unsaturated fatty acid, ester, or carboxylate salt has a straight alkene chain and can be represented by the general formula: CH₃—(CH₂)_(n1)—[—(CH₂)_(n3)—CH═CH—]_(x)—(CH₂)_(n2)—COOR

where:

-   -   R is hydrogen (fatty acid), an aliphatic group (fatty ester), or         a metal ion (carboxylate salt);     -   n1 is an integer equal to or greater than 0 (typically 0 to 15;         more typically 0, 3, or 6);     -   n2 is an integer equal to or greater than 0 (typically 2 to 11;         more typically 3, 4, 7, 9, or 11);     -   n3 is an integer equal to or greater than 0 (typically 0 to 6;         more typically 1); and     -   x is an integer equal to or greater than 1 (typically 1 to 6,         more typically 1 to 3).

A summary of some unsaturated fatty acids and esters is provided in TABLE A.

TABLE A Unsaturated Fatty Acids/Esters Examples Examples of fatty of fatty Type General Formula acids esters Monounsaturated CH₃—(CH₂)_(n1)—[—(CH₂)_(n3)—CH═CH—]_(x)—(CH₂)_(n2)— Oleic Methyl COOR Acid Oleate Where x is 1, and n1, n2, n3, and R are as described (x = 1, (x = 1. above. n1 = 6; n1 = 6; n2 = 7; n2 = 7; n3 = 1; n3 = 1; and R is and R is H.) CH3.) Polyunsaturated Diunsaturated Linoleic Methyl CH₃—(CH₂)_(n1)—[—(CH₂)_(n3)—CH═CH—]_(x)—(CH₂)_(n2)— acid Linoleate COOR (x = 2, (x = 2, Where x is 2, and n1, n2, n3, and R are as described n1 = 3; n1 = 3; above. n2 = 7; n2 = 7; n3 = 1; n3 = 1; and R is and R is H.) CH3.) Triunsaturated Linolenic Methyl CH₃—(CH₂)_(n1)—[—(CH₂)_(n3)—CH═CH—]_(x)—(CH₂)_(n2)— acid Linolenate COOR (x = 3, (x = 3, Where x is 3, and n1, n2, n3, and R are as described n1 = 0; n1 = 0; above. n2 = 7; n2 = 7; n3 = 1; n3 = 1; and R is and R is H.) CH3.)

Unsaturated monoesters may be alkyl esters (e.g., methyl esters) or aryl esters and may be derived from unsaturated fatty acids or unsaturated glycerides by transesterifying with a monohydric alcohol. The monohydric alcohol may be any monohydric alcohol that is capable of reacting with the unsaturated free fatty acid or unsaturated glyceride to form the corresponding unsaturated monoester. In some embodiments, the monohydric alcohol is a C1 to C20 monohydric alcohol, for example, a C1 to C12 monohydric alcohol, a C1 to C8 monohydric alcohol, or a C1 to C4 monohydric alcohol. The carbon atoms of the monohydric alcohol may be arranged in a straight chain or in a branched chain structure, and may be substituted with one or more substituents. Representative examples of monohydric alcohols include methanol, ethanol, propanol (e.g., isopropanol), and butanol.

Transesterification of an unsaturated triglyceride can be represented as follows. 1 Unsaturated Triglyceride+3 Alcohol→1 Glycerol+3 Monoesters

Depending upon the make-up of the unsaturated triglyceride, the above reaction may yield one, two, or three moles of unsaturated monoester. Transesterification is typically conducted in the presence of a catalyst, for example, alkali catalysts, acid catalysts, or enzymes. Representative alkali transesterification catalysts include NaOH, KOH, sodium and potassium alkoxides (e.g., sodium methoxide), sodium ethoxide, sodium propoxide, sodium butoxide. Representative acid catalysts include sulfuric acid, phosphoric acid, hydrochloric acid, and sulfonic acids. Heterogeneous catalysts may also be used for transesterification. These include alkaline earth metals or their salts such as CaO, MgO, calcium acetate, barium acetate, natural clays, zeolites, Sn, Ge or Pb, supported on various materials such as ZnO, MgO, TiO₂, activated carbon or graphite, and inorganic oxides such as alumina, silica-alumina, boria, oxides of P, Ti, Zr, Cr, Zn, Mg, Ca, and Fe. In exemplary embodiments, the triglyceride is transesterified with methanol (CH₃OH) in order to form free fatty acid methyl esters.

In some embodiments, the unsaturated fatty esters are unsaturated polyol esters. As used herein the term “unsaturated polyol ester” refers to compounds that have at least one unsaturated fatty acid that is esterified to the hydroxyl group of a polyol. The other hydroxyl groups of the polyol may be unreacted, may be esterified with a saturated fatty acid, or may be esterified with an unsaturated fatty acid. The fatty acids in the polyol ester may be linear or branched and may optionally have functional groups other than the carboxylic acid such as one or more hydroxyl groups. Examples of polyols include glycerol, 1,3 propanediol, propylene glycol, erythritol, trimethylolpropane, pentaerythritol, and sorbitol. In many embodiments, unsaturated polyol esters have the general formula: R(O—Y)_(m)(OH)_(n)(O—X)_(b)

where

-   -   R is an organic group having a valency of (n+m+b);     -   m is an integer from 0 to (n+m+b−1), typically 0 to 2;     -   b is an integer from 1 to (n+m+b), typically 1 to 3;     -   n is an integer from 0 to (n+m+b−1), typically 0 to 2;     -   (n+m+b) is an integer that is 2 or greater;     -   X is —(O)C—(CH₂)_(n2)—[—CH═CH—(CH₂)_(n3)—]_(x)—(CH₂)_(n1)—CH₃;     -   Y is —(O)C—R′;     -   R′ is a straight or branched chain alkyl or alkenyl group;     -   n1 is an integer equal to or greater than 0 (typically 0 to 15;         more typically 0, 3, or 6);     -   n2 is an integer equal to or greater than 0 (typically 2 to 11;         more typically 3, 4, 7, 9, or 11);     -   n3 is an integer equal to or greater than 0 (typically 0 to 6;         more typically 1); and     -   x is an integer equal to or greater than 1 (typically 1 to 6,         more typically 1 to 3).

In many embodiments, the unsaturated polyol esters are unsaturated glycerides. As used herein the term “unsaturated glyceride” refers to a polyol ester having at least one (e.g., 1 to 3) unsaturated fatty acid that is esterified with a molecule of glycerol. The fatty acid groups may be linear or branched and may include pendant hydroxyl groups. In many embodiments, the unsaturated glycerides are represented by the general formula: CH₂A-CHB—CH₂C

where

-   -   -A; —B; and —C are selected from     -   —OH;     -   —O(O)C—(CH₂)_(n2)—[—CH═CH—(CH₂)_(n3)—]_(x)—(CH₂)_(n1)—CH₃; and     -   —O(O)C—R′;

with the proviso that at least one of -A, —B, or —C is

-   -   —O(O)C—(CH₂)_(n2)—[—CH═CH—(CH₂)_(n3)—]_(x)—(CH₂)_(n1)—CH₃.

In the above formula:

-   -   R′ is a straight or branched chain alkyl or alkenyl group;     -   n1 is an integer equal to or greater than 0 (typically 0 to 15;         more typically 0, 3, or 6);     -   n2 is an integer equal to or greater than 0 (typically 2 to 11;         more typically 3, 4, 7, 9, or 11);     -   n3 is an integer equal to or greater than 0 (typically 0 to 6;         more typically 1); and     -   x is an integer equal to or greater than 1 (typically 1 to 6,         more typically 1 to 3).

Unsaturated glycerides having two —OH groups (e.g., -A and —B are —OH) are commonly known as unsaturated monoglycerides. Unsaturated glycerides having one —OH group are commonly known as unsaturated diglycerides. Unsaturated glycerides having no —OH groups are commonly known as unsaturated triglycerides.

As shown in the formula above, the unsaturated glyceride may include monounsaturated fatty acids, polyunsaturated fatty acids, and saturated fatty acids that are esterified to the glycerol molecule. The main chain of the individual fatty acids may have the same or different chain lengths. Accordingly, the unsaturated glyceride may contain up to three different fatty acids so long as at least one fatty acid is an unsaturated fatty acid.

In many embodiments, useful starting compositions are derived from natural oils such as plant-based oils or animal fats. Representative examples of plant-based oils include canola oil, rapeseed oil, coconut oil, corn oil, cottonseed oil, olive oil, palm oil, peanut oil, safflower oil, sesame oil, soybean oil, sunflower oil, linseed oil, palm kernel oil, tung oil, castor oil, and the like. Representative examples of animal fats include lard, tallow, chicken fat (yellow grease), and fish oil. Other useful oils include tall oil and algae oil.

In many embodiments, the plant-based oil is soybean oil. Soybean oil comprises unsaturated glycerides, for example, in many embodiments about 95% weight or greater (e.g., 99% weight or greater)triglycerides. Major fatty acids making up soybean oil include saturated fatty acids, for example, palmitic acid (hexadecanoic acid) and stearic acid (octadecanoic acid), and unsaturated fatty acids, for example, oleic acid (9-octadecenoic acid), linoleic acid (9,12-octadecadienoic acid), and linolenic acid (9,12,15-octadecatrienoic acid). Soybean oil is a highly unsaturated vegetable oil with many of the triglyceride molecules having at least two unsaturated fatty acids.

The method of the invention can be used to produce multiple organic acid compounds. As discussed below, the position of the carbon-carbon double bond closest to the carboxylic acid, ester, or carboxylate salt group dictates the chain length of the organic acid compound that is formed by the method of the invention.

Δ9 Starting Compositions:

In many embodiments, the starting composition comprises a Δ9 unsaturated fatty acid, a Δ9 unsaturated fatty ester (e.g., monoesters or polyol esters), a Δ9 unsaturated fatty acid salt, or a mixture of two or more of the foregoing. Δ9 unsaturated starting materials have a carbon-carbon double bond located between the 9^(th) and 10^(th) carbon atoms (i.e., between C9 and C10) in the alkene chain of the unsaturated fatty acid, ester, or salt. In determining this position, the alkene chain is numbered beginning with the carbon atom in the carbonyl group of the unsaturated fatty acid, ester, or salt. Δ9 unsaturated fatty acids, esters, and salts include polyunsaturated fatty acids, esters, or salts (i.e., having more than one carbon-carbon double bond in the alkene chain) so long as one of the carbon-carbon double bonds is located between C9 and C10. For example, included within the definition of Δ9 unsaturated fatty acids, esters, or salts are Δ9, 12 unsaturated fatty acids, esters or salts, and Δ9, 12, 15 unsaturated fatty acids, esters or salts.

In many embodiments, the Δ9 unsaturated starting materials have a straight alkene chain and may be represented by the general structure: CH₃—(CH₂)_(n1)—[—(CH₂)_(n3)—CH═CH—]_(x)—(CH₂)₇—COOR

where

-   -   R is hydrogen (fatty acid), an aliphatic group (fatty monoester)         or a metal ion (carboxylate salt);     -   n1 is an integer equal to or greater than 0 (typically 0 to 6;         more typically 0, 3, 6);     -   n3 is an integer equal to or greater than 0 (typically 1); and     -   x is an integer equal to or greater than 1 (typically 1 to 6,         more typically 1 to 3).

In exemplary embodiments, the Δ9 unsaturated starting materials have a total of 18 carbons in the alkene chain. Examples include CH₃—(CH₂)₇—CH═CH—(CH₂)₇—COOR; CH₃—(CH₂)₄—CH═CH—CH₂—CH═CH—(CH₂)₇—COOR; and CH₃—CH₂—CH═CH—CH₂—CH═CH—CH₂—CH═CH—(CH₂)₇—COOR.

-   -   where R is hydrogen (fatty acid), an aliphatic group (fatty         monoester) or a metal ion (fatty acid salt);

Δ9 unsaturated fatty esters may be monoesters or polyol esters. In many embodiments, the Δ9 unsaturated polyol esters have the general structure CH₂A-CHB—CH₂C

where

-   -   -A; —B; and —C are independently selected from     -   —OH;     -   —O(O)C—R′; and     -   —O(O)C—(CH₂)₇—[—CH═CH—(CH₂)_(n3)—]_(x-)—(CH₂)_(n1)—CH₃;

with the proviso that at least one of -A, —B, or —C is

-   -   —O(O)C—(CH₂)₇—[—CH═CH—(CH₂)_(n3)—]_(x-)—(CH₂)_(n1)—CH₃.

In the above formula:

-   -   R′ is a straight or branched chain alkyl or alkenyl group;     -   n1 is an integer equal to or greater than 0 (typically 0 to 6;         more typically 0, 3, 6);     -   n3 is an integer equal to or greater than 0 (typically 1); and     -   x is an integer equal to or greater than 1 (typically 1 to 6,         more typically 1 to 3).

In exemplary embodiments, the starting composition comprises one or more C18 fatty acids, for example, oleic acid (i.e., 9-octadecenoic acid), linoleic acid (i.e., 9,12-octadecadienoic acid), and linolenic acid (i.e., 9,12,15-octadecatrienoic acid). In other exemplary embodiments, the starting composition comprises one or more C18 fatty esters, for example, methyl oleate, methyl linoleate, and methyl linolenate. In yet another exemplary embodiment, the starting composition comprises an unsaturated glyceride comprising Δ9 fatty acids, for example, C18 Δ9 fatty acids.

Δ9 starting compositions may be derived, for example, from vegetable oils such as soybean oil, rapeseed oil, corn oil, sesame oil, cottonseed oil, sunflower oil, canola oil, safflower oil, palm oil, palm kernel oil, linseed oil, castor oil, olive oil, peanut oil, and the like. Since these vegetable oils yield predominately in glyceride form, the oils are typically processed (e.g., by transesterification) to yield unsaturated free fatty esters, unsaturated free fatty acids, or carboxylate salts thereof. Δ9 starting materials may also be derived from tung oil which typically contains oleic acid, linoleic acid, and eleostearic acid (C18; Δ9, 11, 13) in glyceride form. Δ9 starting materials may also be derived from tall oil, fish oil, lard, and tallow.

Δ5 Starting Compositions:

Also useful as a starting composition in the methods of the present invention are Δ5 unsaturated fatty acids, esters, or salts. As used herein “Δ5” refers to unsaturated fatty acids, esters, or salts having a carbon-carbon double bond located between the 5th and 6th carbon atom in the alkene chain of the unsaturated fatty acid, ester, or salt. In some embodiments, Δ5 unsaturated fatty acids, esters, and salts have the general structure: CH₃—(CH₂)_(n1)—[—(CH₂)_(n3)—CH═CH—]_(x)—(CH₂)₃—COOR

where

-   -   R is hydrogen (fatty acid), an aliphatic group (fatty monoester)         or a metal ion (carboxylate salt);     -   n1 is an integer equal to or greater than 0 (typically 1 to 15;         more typically 1, 13, or 15);     -   n3 is an integer equal to or greater than 0 (typically 0 to 6;         more typically 0 or 6); and     -   x is an integer equal to or greater than 1 (typically 1 to 6,         more typically 1 to 2).

The Δ5 unsaturated fatty esters may be monoesters or polyol esters (e.g., unsaturated glycerides). In many embodiments, the Δ5 unsaturated polyol esters have the general structure: CH₂A-CHB—CH₂C

where

-   -   -A; —B; and —C are independently selected from     -   —OH;     -   —O(O)C—R′; and     -   —O(O)C—(CH₂)₃—[—CH═CH—(CH₂)_(n3)—]_(x)—(CH₂)_(n1)—CH₃;

with the proviso that at least one of -A, —B, or —C is

-   -   —O(O)C—(CH₂)₃—[—CH═CH—(CH₂)_(n3)—]_(x)—(CH₂)_(n1)CH₃.

In the above formula:

-   -   R′ is a straight or branched chain alkyl or alkenyl group;     -   n1 is an integer equal to or greater than 0 (typically 1 to 15;         more typically 1, 13, or 15);     -   n3 is an integer equal to or greater than 0 (typically 0 to 6;         more typically 0 or 6); and     -   x is an integer equal to or greater than 1 (typically 1 to 6,         more typically 1 to 2).

Δ5 starting compositions may be derived, for example, from meadowfoam oil which contains a twenty carbon monounsaturated fatty acid (C20:1; Δ5) in glyceride form. Δ5 starting compositions may also be derived from fish oil which typically contains eicosapentaenoic acid (C20:5; Δ5, 8, 11, 14, 17) in glyceride form.

Δ6 Starting Compositions:

Also useful as a starting composition in the methods of the present invention are Δ6 unsaturated fatty acids, esters, or salts. As used herein “Δ6” refers to unsaturated fatty acids, esters, or salts having a carbon-carbon double bond located between the 6th and 7th carbon atom in the alkene chain of the unsaturated fatty acid, ester, or salt. In some embodiments, Δ6 unsaturated fatty acids, esters, and salts have the general structure: CH₃—(CH₂)_(n1)—[—(CH₂)_(n3)—CH═CH—]_(x)—(CH₂)₄—COOR

where

-   -   R is hydrogen (fatty acid), an aliphatic group (fatty monoester)         or a metal ion (carboxylate salt);     -   n1 is an integer equal to or greater than 0 (typically 0 to 10);     -   n3 is an integer equal to or greater than 0; (typically 0); and     -   x is an integer equal to or greater than 1 (typically 1 to 6,         more typically 1).

The Δ6 unsaturated fatty esters may be monoesters or polyol esters (e.g., unsaturated glycerides). In many embodiments, the Δ6 unsaturated polyol esters have the general structure: CH₂A-CHB—CH₂C

where

-   -   -A; —B; and —C are independently selected from     -   —OH;     -   —O(O)C—R′; and     -   —O(O)C—(CH₂)₄—[—CH═CH—(CH₂)_(n3)—]_(x)—(CH₂)_(n1)—CH₃;

with the proviso that at least one of -A, —B, or —C is

-   -   —O(O)C—(CH₂)₄—[—CH═CH—(CH₂)_(n3)—]_(x)—(CH₂)_(n1)—CH₃.

In the above formula:

-   -   R′ is a straight or branched chain alkyl or alkenyl group;     -   n1 is an integer equal to or greater than 0 (typically 0 to 10);     -   n3 is an integer equal to or greater than 0; (typically 0); and     -   x is an integer equal to or greater than 1 (typically 1 to 6,         more typically 1).

Δ6 starting compositions may be derived from coriander oil which contains an 18 carbon unsaturated fatty acid (C18:1; Δ6) in glyceride form.

Δ11 Starting Compositions:

Also useful as a starting composition in the methods of the present invention are Δ11 unsaturated fatty acids, esters, or salts. As used herein “Δ11” refers to unsaturated fatty acids, esters, or salts having a carbon-carbon double bond located between the 11^(th) and 12^(th) carbon atom in the alkene chain of the unsaturated fatty acid, ester, or salt. In some embodiments, Δ11 unsaturated fatty acids, esters, and salts have the general structure: CH₃—(CH₂)_(n1)—[—(CH₂)_(n3)—CH═CH—]_(x)—(CH₂)₉—COOR

where

-   -   R is hydrogen (fatty acid), an aliphatic group (fatty monoester)         or a metal ion (carboxylate salt);     -   n1 is an integer equal to or greater than 0 (typically 0 to 7;         more typically 7);     -   n3 is an integer equal to or greater than 0 (typically 0); and     -   x is an integer equal to or greater than 1 (typically 1 to 6,         more typically 1).

The Δ11 unsaturated fatty esters may be monoesters or polyol esters (e.g., unsaturated glycerides). In many embodiments, the Δ11 unsaturated polyol esters have the general structure: CH₂A-CHB—CH₂C

where

-   -   -A; —B; and —C are independently selected from     -   —OH;     -   —O(O)C—R′; and     -   —O(O)C—(CH₂)₉—[—CH═CH—(CH₂)_(n3)—]_(x)—(CH₂)_(n1)CH₃;

with the proviso that at least one of -A, —B, or —C is

-   -   —O(O)C—(CH₂)₉—[—CH═CH—(CH₂)_(n3)—]_(x)—(CH₂)_(n1)CH₃.

In the above formula:

-   -   R′ is a straight or branched chain alkyl or alkenyl group;     -   n¹ is an integer equal to or greater than 0 (typically 0 to 7;         more typically 7);     -   n3 is an integer equal to or greater than 0 (typically 0); and     -   x is an integer equal to or greater than 1 (typically 1 to 6,         more typically 1).

Sources of Δ11 starting compositions include camelina oil which contains gondoic acid (C20:1 Δ11) at approximately 15% of the fatty acid composition.

Δ13 Starting Compositions:

Also useful as a starting composition in the methods of the present invention are Δ13 unsaturated fatty acids, esters, or salts. As used herein “Δ13” refers to unsaturated fatty acids, esters, or salts having a carbon-carbon double bond located between the 13^(th) and 14^(th) carbon atom in the alkene chain of the unsaturated fatty acid, ester, or salt. In some embodiments, Δ13 unsaturated fatty acids, esters, and salts have the general structure: CH₃—(CH₂)_(n1)—[—(CH₂)_(n3)—CH═CH—]_(x)—(CH₂)₁₁—COOR

where

-   -   R is hydrogen (fatty acid), an aliphatic group (fatty monoester)         or a metal ion (carboxylate salt);     -   n1 is an integer equal to or greater than 0 (typically 7);     -   n3 is an integer equal to or greater than 0 (typically 0)     -   x is an integer equal to or greater than 1 (typically 1 to 6,         more typically 1).

The Δ13 unsaturated fatty esters may be monoesters or polyol esters (e.g., unsaturated glycerides). In many embodiments, the Δ13 unsaturated polyol esters have the general structure CH₂A-CHB—CH₂C

where

-   -   -A; —B; and —C are independently selected from     -   —OH;     -   —O(O)C—R′; and     -   —O(O)C—(CH₂)₁₁—[—CH═CH—(CH₂)_(n3)—]_(x)—(CH₂)_(n1)—CH₃,

with the proviso that at least one of -A, —B, or —C is

-   -   —O(O)C—(CH₂)₁₁—[—CH═CH—(CH₂)_(n3)—]_(x)—(CH₂)_(n1)—CH₃.

In the above formula:

-   -   R′ is a straight or branched chain alkyl or alkenyl group;     -   n1 is an integer equal to or greater than 0 (typically 7);     -   n3 is an integer equal to or greater than 0 (typically 0)     -   x is an integer equal to or greater than 1 (typically 1 to 6,         more typically 1).

Sources of Δ13 starting compositions include crambe oil, fish oil, and high erucic acid rapeseed oil which are high in erucic acid (C22:1 Δ13) in glyceride form.

Other useful starting compositions include, for example, Δ8 and Δ4 starting materials. Δ4 starting materials may be obtained, for example, from fish oil which typically includes an amount of docosahexaenoic acid (C22:6; Δ4, 7, 10, 13, 16, 19). Δ8 starting materials may also be obtained from fish oil which typically includes an amount of eicosatetraenoic acid (C20:4; Δ8, 11, 14, 17).

A summary of some useful starting compositions is provided in TABLE B.

TABLE B Starting Bond Composition Description Classification Locations Oleic acid C18 monounsaturated Δ9 Δ9 fatty acid (C18:1) Linoleic acid C18 diunsaturated fatty Δ9 Δ9, 12 acid (C18:2) Linolenic acid C18 triunsaturated fatty Δ9 Δ9, 12, 15 acid (C18:3) Alkyl oleate C18 monounsaturated Δ9 Δ9 fatty ester (C18:1) Alkyl linoleate C18 diunsaturated fatty Δ9 Δ9, 12 ester (C18:2) Alkyl linolenate C18 triunsaturated fatty Δ9 Δ9, 12, 15 ester (C18:3) Vegetable Oil Unsaturated glycerides Δ9 Δ9 (e.g., soybean of C18:1, C18:2, and Δ9, 12 oil) C18:3 fatty acids Δ9, 12, 15 Tung Oil Unsaturated glycerides Δ9 Δ9, 11, 13 of C18:1; C18:2; and Δ9 C18:3 fatty acids Δ9, 12 Meadowfoam Unsaturated glycerides Δ5 Δ5 Oil of C20:1 fatty acids. Coriander Oil Unsaturated glycerides Δ6 Δ6 of C18:1 fatty acids. Camelina oil Unsaturated glycerides Δ11  Δ11  of C20:1 fatty acids Crambe Oil or Unsaturated glycerides Δ13  Δ13  High Erucic of C22:1 fatty acids Rapeseed Oil Cross-Metathesis (Step (b)):

According to the method of the invention, the starting composition is cross-metathesized with a short-chain olefin in the presence of a metathesis catalyst to form cross-metathesis products comprising: (i) one or more olefin compounds; and (ii) one or more acid-, ester-, or carboxylate salt-functionalized alkenes having at least one carbon-carbon double bond.

Short-chain olefins are short chain length organic compounds that have at least one carbon-carbon double bond. In many embodiments, the short chain olefins have between about 4 and about 9 carbon atoms. Short chain olefins can be represented by the structure (II): R⁷R⁸C═CR⁹R¹⁰  (II)

-   -   where R⁷, R⁸, R⁹, and R¹⁰ are each, independently, hydrogen or         an organic group, with the proviso that at least one of R⁷ or R⁸         is an organic group.

The organic group may be an aliphatic group, an alicyclic group, or an aromatic group. Organic groups may optionally include heteroatoms (e.g., O, N, or S atoms), as well as functional groups (e.g., carbonyl groups). The term aliphatic group means a saturated or unsaturated, linear or branched, hydrocarbon group. This term is used to encompass alkyl groups. The term alkyl group means a monovalent, saturated, linear, branched, or cyclic hydrocarbon group. Representative examples of alkyl groups include methyl, ethyl, propyl (n-propyl or i-propyl), butyl (n-butyl or t-butyl), pentyl, hexyl, and heptyl. An alicyclic group is an aliphatic group arranged in one or more closed ring structures. The term is used to encompass saturated (i.e., cycloparaffins) or unsaturated (cycloolefins or cycloacetylenes) groups. An aromatic or aryl group is an unsaturated cyclic hydrocarbon having a conjugated ring structure. Included within aromatic or aryl groups are those possessing both an aromatic ring structure and an aliphatic or alicyclic group.

In many embodiments, the short-chain olefin is a short-chain internal olefin. Short-chain internal olefins may be represented by structure (II): R⁷R⁸C═CR⁹R¹⁰  (II)

-   -   where R⁷, R⁸, R⁹, and R¹⁰ are each, independently, hydrogen or         an organic group, with the proviso that at least one of R⁷ or R⁸         is an organic group, and at least one of R⁹ or R¹⁰ is an organic         group.

Short-chain internal olefins may be symmetric or asymmetric. Symmetric short-chain internal olefins having one carbon-carbon double bond may be represented by structure (II-A): R⁷CH═CHR⁹  (II-A)

-   -   where —R⁷ and —R⁹ are same organic group.

Representative examples of symmetric short-chain internal olefins include 2-butene, 3-hexene, and 4-octene. In some embodiments, the short-chain internal olefin is asymmetric. Representative examples of asymmetric short-chain internal olefins include 2-pentene, 2-hexene, 2-heptene, 3-heptene, 2-octene, 3-octene, 2-nonene, 3-nonene, and 4-nonene.

In many embodiments, symmetric short-chain internal olefins are preferred for cross-metathesis because the cross-metathesis products that result will include fewer products than if an asymmetric short-chain internal olefin is used for cross-metathesis. For example, as shown below, when a first double-bond containing compound (i.e., A=B) is cross-metathesized with a symmetric short-chain internal olefin (i.e., represented by C═C), two cross-metathesis products are produced. By contrast, when the same double-bond containing compound is cross-metathesized with an asymmetric short-chain internal olefin (i.e., represented by C=D), four cross-metathesis products are produced.

Metathesis of Symmetric Short-chain Internal Olefin (C═C) A=B+C═C

A=C+B═C

Metathesis of Asymmetric Short-chain Internal Olefin (C=D): A=B+C=D

A=C+B═C+A=D+B=D

In some embodiments, the short-chain olefin is an α-olefin. Alpha olefins are included in general structure (II) when R⁷, R⁸, and R⁹ are all hydrogen. Representative α-olefin are shown in general structure (II-B): CH₂═CH—R¹⁰  (II-B)

-   -   where —R¹⁰ is an organic group.

Representative —R¹⁰ groups include —(CH₂)_(n)—CH₃, where n ranges from 0 to 6. Exemplary alpha olefin compounds include 1-propene, 1-butene, 1-pentene, 1-hexene, 1-heptene, 1-octene, and 1-nonene.

Metathesis Catalysts:

Metathesis reactions proceed in the presence of a catalytically effective amount of a metathesis catalyst. The term “metathesis catalyst” includes any catalyst or catalyst system which catalyzes the olefin metathesis reaction.

Any known or future-developed metathesis catalyst may be used, alone or in combination with one or more additional catalysts, in accordance with embodiments of the present method. Exemplary metathesis catalysts include metal carbene catalysts based upon transition metals, for example, ruthenium, molybdenum, osmium, chromium, rhenium, and tungsten. In certain embodiments, the metathesis catalyst is preferably a Group 8 transition metal complex having the structure of formula (III)

in which the various substituents are as follows:

-   -   M is a Group 8 transition metal;     -   L¹, L² and L³ are neutral electron donor ligands;     -   n is 0 or 1, such that L³ may or may not be present;     -   m is 0, 1, or 2;     -   X¹ and X² are anionic ligands; and     -   R¹ and R² are independently selected from hydrogen, hydrocarbyl,         substituted hydrocarbyl, heteroatom-containing hydrocarbyl,         substituted heteroatom-containing hydrocarbyl, and functional         groups,

wherein any two or more of X¹, X², L¹, L², L³, R¹, and R² can be taken together to form a cyclic group, and further wherein any one or more of X¹, X², L¹, L², L³, R¹, and R² may be attached to a support.

Preferred catalysts contain Ru or Os as the Group 8 transition metal, with Ru particularly preferred.

Numerous embodiments of the catalysts useful in the reactions of the disclosure are described in more detail infra. For the sake of convenience, the catalysts are described in groups, but it should be emphasized that these groups are not meant to be limiting in any way. That is, any of the catalysts useful in the disclosure may fit the description of more than one of the groups described herein.

A first group of catalysts, then, are commonly referred to as 1^(st) Generation Grubbs-type catalysts, and have the structure of formula (III). For the first group of catalysts, M and m are as described above, and n, X¹, X², L¹, L², L³, R¹, and R² are described as follows.

For the first group of catalysts, n is 0, and L¹ and L² are independently selected from phosphine, sulfonated phosphine, phosphite, phosphinite, phosphonite, arsine, stibine, ether, amine, amide, imine, sulfoxide, carboxyl, nitrosyl, pyridine, substituted pyridine, imidazole, substituted imidazole, pyrazine, and thioether. Exemplary ligands are trisubstituted phosphines.

X¹ and X² are anionic ligands, and may be the same or different, or are linked together to form a cyclic group, typically although not necessarily a five- to eight-membered ring. In preferred embodiments, X¹ and X² are each independently hydrogen, halide, or one of the following groups: C₁-C₂₀ alkyl, C₅-C₂₄ aryl, C₁-C₂₀ alkoxy, C₅-C₂₄ aryloxy, C₂-C₂₀ alkoxycarbonyl, C₆-C₂₄ aryloxycarbonyl, C₂-C₂₄ acyl, C₂-C₂₄ acyloxy, C₁-C₂₀ alkylsulfonato, C₅-C₂₄ arylsulfonato, C₁-C₂₀ alkylsulfanyl, C₅-C₂₄ arylsulfanyl, C₁-C₂₀ alkylsulfinyl, or C₅-C₂₄ arylsulfinyl. Optionally, X¹ and X² may be substituted with one or more moieties selected from C₁-C₁₂ alkyl, C₁-C₁₂ alkoxy, C₅-C₂₄ aryl, and halide, which may, in turn, with the exception of halide, be further substituted with one or more groups selected from halide, C₁-C₆ alkyl, C₁-C₆ alkoxy, and phenyl. In more preferred embodiments, X¹ and X² are halide, benzoate, C₂-C₆ acyl, C₂-C₆ alkoxycarbonyl, C₁-C₆ alkyl, phenoxy, C₁-C₆ alkoxy, C₁-C₆ alkylsulfanyl, aryl, or C₁-C₆ alkylsulfonyl. In even more preferred embodiments, X¹ and X² are each halide, CF₃CO₂, CH₃CO₂, CFH₂CO₂, (CH₃)₃CO, (CF₃)₂(CH₃)CO, (CF₃)(CH₃)₂CO, PhO, MeO, EtO, tosylate, mesylate, or trifluoromethane-sulfonate. In the most preferred embodiments, X¹ and X² are each chloride.

R¹ and R² are independently selected from hydrogen, hydrocarbyl (e.g., C₁-C₂₀ alkyl, C₂-C₂₀ alkenyl, C₂-C₂₀ alkynyl, C₅-C₂₄ aryl, C₆-C₂₄ alkaryl, C₆-C₂₄ aralkyl, etc.), substituted hydrocarbyl (e.g., substituted C₁-C₂₀ alkyl, C₂-C₂₀ alkenyl, C₂-C₂₀ alkynyl, C₅-C₂₄ aryl, C₆-C₂₄ alkaryl, C₆-C₂₄ aralkyl, etc.), heteroatom-containing hydrocarbyl (e.g., heteroatom-containing C₁-C₂₀ alkyl, C₂-C₂₀ alkenyl, C₂-C₂₀ alkynyl, C₅-C₂₄ aryl, C₆-C₂₄ alkaryl, C₆-C₂₄ aralkyl, etc.), and substituted heteroatom-containing hydrocarbyl (e.g., substituted heteroatom-containing C₁-C₂₀ alkyl, C₂-C₂₀ alkenyl, C₂-C₂₀ alkynyl, C₅-C₂₄ aryl, C₆-C₂₄ alkaryl, C₆-C₂₄ aralkyl, etc.), and functional groups. R¹ and R² may also be linked to form a cyclic group, which may be aliphatic or aromatic, and may contain substituents and/or heteroatoms. Generally, such a cyclic group will contain 4 to 12, preferably 5, 6, 7, or 8 ring atoms.

In preferred catalysts, R¹ is hydrogen and R² is selected from C₁-C₂₀ alkyl, C₂-C₂₀ alkenyl, and C₅-C₂₄ aryl, more preferably C₁-C₆ alkyl, C₂-C₆ alkenyl, and C₅-C₁₄ aryl. Still more preferably, R² is phenyl, vinyl, methyl, isopropyl, or t-butyl, optionally substituted with one or more moieties selected from C₁-C₆ alkyl, C₁-C₆ alkoxy, phenyl, and a functional group Fn as defined earlier herein. Most preferably, R² is phenyl or vinyl substituted with one or more moieties selected from methyl, ethyl, chloro, bromo, iodo, fluoro, nitro, dimethylamino, methyl, methoxy, and phenyl. Optimally, R² is phenyl or —C═C(CH₃)₂.

Any two or more (typically two, three, or four) of X¹, X², L¹, L², L³, R¹, and R² can be taken together to form a cyclic group, as disclosed, for example, in U.S. Pat. No. 5,312,940 to Grubbs et al. When any of X¹, X², L¹, L², L³, R¹, and R² are linked to form cyclic groups, those cyclic groups may contain 4 to 12, preferably 4, 5, 6, 7 or 8 atoms, or may comprise two or three of such rings, which may be either fused or linked. The cyclic groups may be aliphatic or aromatic, and may be heteroatom-containing and/or substituted. The cyclic group may, in some cases, form a bidentate ligand or a tridentate ligand. Examples of bidentate ligands include, but are not limited to, bisphosphines, dialkoxides, alkyldiketonates, and aryldiketonates.

A second group of catalysts, commonly referred to as 2^(nd) Generation Grubbs-type catalysts, have the structure of formula (III), wherein L¹ is a carbene ligand having the structure of formula (IV)

such that the complex may have the structure of formula (V)

wherein M, m, n, X¹, X², L², L³, R¹, and R² are as defined for the first group of catalysts, and the remaining substituents are as follows.

X and Y are heteroatoms typically selected from N, O, S, and P. Since O and S are divalent, p is necessarily zero when X is O or S, and q is necessarily zero when Y is O or S. However, when X is N or P, then p is 1, and when Y is N or P, then q is 1. In a preferred embodiment, both X and Y are N.

Q¹, Q², Q³, and Q⁴ are linkers, e.g., hydrocarbylene (including substituted hydrocarbylene, heteroatom-containing hydrocarbylene, and substituted heteroatom-containing hydrocarbylene, such as substituted and/or heteroatom-containing alkylene) or —(CO)—, and w, x, y, and z are independently zero or 1, meaning that each linker is optional. Preferably, w, x, y, and z are all zero. Further, two or more substituents on adjacent atoms within Q¹, Q², Q³, and Q⁴ may be linked to form an additional cyclic group.

R³, R^(3A), R⁴, and R^(4A) are independently selected from hydrogen, hydrocarbyl, substituted hydrocarbyl, heteroatom-containing hydrocarbyl, and substituted heteroatom-contain ing hydrocarbyl.

In addition, any two or more of X¹, X², L¹, L², L³, R¹, R², R³, R^(3A), R⁴, and R^(4A) can be taken together to form a cyclic group, and any one or more of X¹, X², L¹, L², L³, R¹, R², R³, R^(3A), R⁴, and R^(4A) may be attached to a support.

Preferably, R^(3A) and R^(4A) are linked to form a cyclic group so that the carbene ligand is an heterocyclic carbene and preferably an N-heterocyclic carbene, such as the N-heterocylic carbene having the structure of formula (VI):

where R³ and R⁴ are defined above, with preferably at least one of R³ and R⁴, and more preferably both R³ and R⁴, being alicyclic or aromatic of one to about five rings, and optionally containing one or more heteroatoms and/or substituents. Q is a linker, typically a hydrocarbylene linker, including substituted hydrocarbylene, heteroatom-containing hydrocarbylene, and substituted heteroatom-containing hydrocarbylene linkers, wherein two or more substituents on adjacent atoms within Q may also be linked to form an additional cyclic structure, which may be similarly substituted to provide a fused polycyclic structure of two to about five cyclic groups. Q is often, although again not necessarily, a two-atom linkage or a three-atom linkage.

Examples of N-heterocyclic carbene ligands suitable as L¹ thus include, but are not limited to, the following:

When M is ruthenium, then, the preferred complexes have the structure of formula (VII).

In a more preferred embodiment, Q is a two-atom linkage having the structure —CR¹¹R¹²CR¹³R¹⁴— or —CR¹¹═CR¹³—, preferably —CR¹¹R¹²—CR¹³R¹⁴—, wherein R¹¹, R¹², R¹³, and R¹⁴ are independently selected from hydrogen, hydrocarbyl, substituted hydrocarbyl, heteroatom-containing hydrocarbyl, substituted heteroatom-containing hydrocarbyl, and functional groups. Examples of functional groups here include carboxyl, C₁-C₂₀ alkoxy, C₅-C₂₄ aryloxy, C₂-C₂₀ alkoxycarbonyl, C₅-C₂₄ alkoxycarbonyl, C₂-C₂₄ acyloxy, C₁-C₂₀ alkylthio, C₅-C₂₄ arylthio, C₁-C₂₀ alkylsulfonyl, and C₁-C₂₀ alkylsulfinyl, optionally substituted with one or more moieties selected from C₁-C₁₂ alkyl, C₁-C₁₂ alkoxy, C₅-C₁₄ aryl, hydroxyl, sulfhydryl, formyl, and halide. R¹¹, R¹², R¹³, and R¹⁴ are preferably independently selected from hydrogen, C₁-C₁₂ alkyl, substituted C₁-C₁₂ alkyl, C₁-C₁₂ heteroalkyl, substituted C₁-C₁₂ heteroalkyl, phenyl, and substituted phenyl. Alternatively, any two of R¹¹, R¹², R¹³, and R¹⁴ may be linked together to form a substituted or unsubstituted, saturated or unsaturated ring structure, e.g., a C₄-C₁₂ alicyclic group or a C₅ or C₆ aryl group, which may itself be substituted, e.g., with linked or fused alicyclic or aromatic groups, or with other substituents.

When R³ and R⁴ are aromatic, they are typically although not necessarily composed of one or two aromatic rings, which may or may not be substituted, e.g., R³ and R⁴ may be phenyl, substituted phenyl, biphenyl, substituted biphenyl, or the like. In one preferred embodiment, R³ and R⁴ are the same and are each unsubstituted phenyl or phenyl substituted with up to three substituents selected from C₁-C₂₀ alkyl, substituted C₁-C₂₀ alkyl, C₁-C₂₀ heteroalkyl, substituted C₁-C₂₀ heteroalkyl, C₅-C₂₄ aryl, substituted C₅-C₂₄ aryl, C₅-C₂₄ heteroaryl, C₆-C₂₄ aralkyl, C₆-C₂₄ alkaryl, or halide. Preferably, any substituents present are hydrogen, C₁-C₁₂ alkyl, C₁-C₁₂ alkoxy, C₅-C₁₄ aryl, substituted C₅-C₁₄ aryl, or halide. As an example, R³ and R⁴ are mesityl.

In a third group of catalysts having the structure of formula (III), M, m, n, X¹, X², R¹, and R² are as defined for the first group of catalysts, L¹ is a strongly coordinating neutral electron donor ligand such as any of those described for the first and second groups of catalysts, and L² and L³ are weakly coordinating neutral electron donor ligands in the form of optionally substituted heterocyclic groups. Again, n is zero or 1, such that L³ may or may not be present. Generally, in the third group of catalysts, L² and L³ are optionally substituted five- or six-membered monocyclic groups containing 1 to 4, preferably 1 to 3, most preferably 1 to 2 heteroatoms, or are optionally substituted bicyclic or polycyclic structures composed of 2 to 5 such five- or six-membered monocyclic groups. If the heterocyclic group is substituted, it should not be substituted on a coordinating heteroatom, and any one cyclic moiety within a heterocyclic group will generally not be substituted with more than 3 substituents.

For the third group of catalysts, examples of L² and L³ include, without limitation, heterocycles containing nitrogen, sulfur, oxygen, or a mixture thereof.

Examples of nitrogen-containing heterocycles appropriate for L² and L³ include pyridine, bipyridine, pyridazine, pyrimidine, bipyridamine, pyrazine, 1,3,5-triazine, 1,2,4-triazine, 1,2,3-triazine, pyrrole, 2H-pyrrole, 3H-pyrrole, pyrazole, 2H-imidazole, 1,2,3-triazole, 1,2,4-triazole, indole, 3H-indole, 1H-isoindole, cyclopenta(b)pyridine, indazole, quinoline, bisquinoline, isoquinoline, bisisoquinoline, cinnoline, quinazoline, naphthyridine, piperidine, piperazine, pyrrolidine, pyrazolidine, quinuclidine, imidazolidine, picolylimine, purine, benzimidazole, bisimidazole, phenazine, acridine, and carbazole.

Examples of sulfur-containing heterocycles appropriate for L² and L³ include thiophene, 1,2-dithiole, 1,3-dithiole, thiepin, benzo(b)thiophene, benzo(c)thiophene, thionaphthene, dibenzothiophene, 2H-thiopyran, 4H-thiopyran, and thioanthrene.

Examples of oxygen-containing heterocycles appropriate for L² and L³ include 2H-pyran, 4H-pyran, 2-pyrone, 4-pyrone, 1,2-dioxin, 1,3-dioxin, oxepin, furan, 2H-1-benzopyran, coumarin, coumarone, chromene, chroman-4-one, isochromen-1-one, isochromen-3-one, xanthene, tetrahydrofuran, 1,4-dioxan, and dibenzofuran.

Examples of mixed heterocycles appropriate for L² and L³ include isoxazole, oxazole, thiazole, isothiazole, 1,2,3-oxadiazole, 1,2,4-oxadiazole, 1,3,4-oxadiazole, 1,2,3,4-oxatriazole, 1,2,3,5-oxatriazole, 3H-1,2,3-dioxazole, 3H-1,2-oxathiole, 1,3-oxathiole, 4H-1,2-oxazine, 2H-1,3-oxazine, 1,4-oxazine, 1,2,5-oxathiazine, o-isooxazine, phenoxazine, phenothiazine, pyrano[3,4-b]pyrrole, indoxazine, benzoxazole, anthranil, and morpholine.

Preferred L² and L³ ligands are aromatic nitrogen-containing and oxygen-containing heterocycles, and particularly preferred L² and L³ ligands are monocyclic N-heteroaryl ligands that are optionally substituted with 1 to 3, preferably 1 or 2, substituents. Specific examples of particularly preferred L² and L³ ligands are pyridine and substituted pyridines, such as 3-bromopyridine, 4-bromopyridine, 3,5-dibromopyridine, 2,4,6-tribromopyridine, 2,6-dibromopyridine, 3-chloropyridine, 4-chloropyridine, 3,5-dichloropyridine, 2,4,6-trichloropyridine, 2,6-dichloropyridine, 4-iodopyridine, 3,5-diiodopyridine, 3,5-dibromo-4-methylpyridine, 3,5-dichloro-4-methylpyridine, 3,5-dimethyl-4-bromopyridine, 3,5-dimethylpyridine, 4-methylpyridine, 3,5-diisopropylpyridine, 2,4,6-trimethylpyridine, 2,4,6-triisopropylpyridine, 4-(tert-butyl)pyridine, 4-phenylpyridine, 3,5-diphenylpyridine, 3,5-dichloro-4-phenylpyridine, and the like.

In general, any substituents present on L² and/or L³ are selected from halo, C₁-C₂₀ alkyl, substituted C₁-C₂₀ alkyl, C₁-C₂₀ heteroalkyl, substituted C₁-C₂₀ heteroalkyl, C₅-C₂₄ aryl, substituted C₅-C₂₄ aryl, C₅-C₂₄ heteroaryl, substituted C₅-C₂₄ heteroaryl, C₆-C₂₄ alkaryl, substituted C₆-C₂₄ alkaryl, C₆-C₂₄ heteroalkaryl, substituted C₆-C₂₄ heteroalkaryl, C₆-C₂₄ aralkyl, substituted C₆-C₂₄ aralkyl, C₆-C₂₄ heteroaralkyl, substituted C₆-C₂₄ heteroaralkyl, and functional groups, with suitable functional groups including, without limitation, C₁-C₂₀ alkoxy, C₅-C₂₄ aryloxy, C₂-C₂₀ alkylcarbonyl, C₆-C₂₄ arylcarbonyl, C₂-C₂₀ alkylcarbonyloxy, C₆-C₂₄ arylcarbonyloxy, C₂-C₂₀ alkoxycarbonyl, C₆-C₂₄ aryloxycarbonyl, halocarbonyl, C₂-C₂₀ alkylcarbonato, C₆-C₂₄ arylcarbonato, carboxy, carboxylato, carbamoyl, mono-(C₁-C₂₀ alkyl)-substituted carbamoyl, di-(C₁-C₂₀ alkyl)-substituted carbamoyl, di-N—(C₁-C₂₀ alkyl), N—(C₅-C₂₄ aryl)-substituted carbamoyl, mono-(C₅-C₂₄ aryl)-substituted carbamoyl, di-(C₆-C₂₄ aryl)-substituted carbamoyl, thiocarbamoyl, mono-(C₁-C₂₀ alkyl)-substituted thiocarbamoyl, di-(C₁-C₂₀ alkyl)-substituted thiocarbamoyl, di-N—(C₁-C₂₀ alkyl)-N—(C₆-C₂₄ aryl)-substituted thiocarbamoyl, mono-(C₆-C₂₄ aryl)-substituted thiocarbamoyl, di-(C₆-C₂₄ aryl)-substituted thiocarbamoyl, carbamido, formyl, thioformyl, amino, mono-(C₁-C₂₀ alkyl)-substituted amino, di-(C₁-C₂₀ alkyl)-substituted amino, mono-(C₅-C₂₄ aryl)-substituted amino, di-(C₅-C₂₄ aryl)-substituted amino, di-N—(C₁-C₂₀ alkyl)-N—(C₅-C₂₄ aryl)-substituted amino, C₂-C₂₀ alkylamido, C₆-C₂₄ arylamido, imino, C₁-C₂₀ alkylimino, C₅-C₂₄ arylimino, nitro, and nitroso. In addition, two adjacent substituents may be taken together to form a ring, generally a five- or six-membered alicyclic or aryl ring, optionally containing 1 to 3 heteroatoms and 1 to 3 substituents as above.

Preferred substituents on L² and L³ include, without limitation, halo, C₁-C₁₂ alkyl, substituted C₁-C₁₂ alkyl, C₁-C₁₂ heteroalkyl, substituted C₁-C₁₂ heteroalkyl, C₅-C₁₄ aryl, substituted C₅-C₁₄ aryl, C₅-C₁₄ heteroaryl, substituted C₅-C₁₄ heteroaryl, C₆-C₁₆ alkaryl, substituted C₆-C₁₆ alkaryl, C₆-C₁₆ heteroalkaryl, substituted C₆-C₁₆ heteroalkaryl, C₆-C₁₆ aralkyl, substituted C₆-C₁₆ aralkyl, C₆-C₁₆ heteroaralkyl, substituted C₆-C₁₆ heteroaralkyl, C₁-C₁₂ alkoxy, C₅-C₁₄ aryloxy, C₂-C₁₂ alkylcarbonyl, C₆-C₁₄ arylcarbonyl, C₂-C₁₂ alkylcarbonyloxy, C₆-C₁₄ arylcarbonyloxy, C₂-C₁₂ alkoxycarbonyl, C₆-C₁₄ aryloxycarbonyl, halocarbonyl, formyl, amino, mono-(C₁-C₁₂ alkyl)-substituted amino, di-(C₁-C₁₂ alkyl)-substituted amino, mono-(C₅-C₁₄ aryl)-substituted amino, di-(C₅-C₁₄ aryl)-substituted amino, and nitro.

Of the foregoing, the most preferred substituents are halo, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ alkoxy, phenyl, substituted phenyl, formyl, N,N-diC₁-C₆ alkyl)amino, nitro, and nitrogen heterocycles as described above (including, for example, pyrrolidine, piperidine, piperazine, pyrazine, pyrimidine, pyridine, pyridazine, etc.).

L² and L³ may also be taken together to form a bidentate or multidentate ligand containing two or more, generally two, coordinating heteroatoms such as N, O, S, or P, with preferred such ligands being diimine ligands of the Brookhart type. One representative bidentate ligand has the structure of formula (VIII)

wherein R¹⁵, R¹⁶, R¹⁷, and R¹⁸ hydrocarbyl (e.g., C₁-C₂₀ alkyl, C₂-C₂₀ alkenyl, C₂-C₂₀ alkynyl, C₅-C₂₄ aryl, C₆-C₂₄ alkaryl, or C₆-C₂₄ aralkyl), substituted hydrocarbyl (e.g., substituted C₁-C₂₀ alkyl, C₂-C₂₀ alkenyl, C₂-C₂₀ alkynyl, C₅-C₂₄ aryl, C₆-C₂₄ alkaryl, or C₆-C₂₄ aralkyl), heteroatom-containing hydrocarbyl (e.g., C₁-C₂₀ heteroalkyl, C₅-C₂₄ heteroaryl, heteroatom-containing C₆-C₂₄ aralkyl, or heteroatom-containing C₆-C₂₄ alkaryl), or substituted heteroatom-containing hydrocarbyl (e.g., substituted C₁-C₂₀ heteroalkyl, C₅-C₂₄ heteroaryl, heteroatom-containing C₆-C₂₄ aralkyl, or heteroatom-containing C₆-C₂₄ alkaryl), or (1) R¹⁵ and R¹⁶, (2) R¹⁷ and R¹⁸, (3) R¹⁶ and R¹⁷, or (4) both R¹⁵ and R¹⁶, and R¹⁷ and R¹⁸, may be taken together to form a ring, i.e., an N-heterocycle. Preferred cyclic groups in such a case are five- and six-membered rings, typically aromatic rings.

In a fourth group of catalysts that have the structure of formula (III), two of the substituents are taken together to form a bidentate ligand or a tridentate ligand. Examples of bidentate ligands include, but are not limited to, bisphosphines, dialkoxides, alkyldiketonates, and aryldiketonates. Specific examples include —P(Ph)₂CH₂CH₂P(Ph)₂-, —As(Ph)₂CH₂CH₂As(Ph₂)—, —P(Ph)₂CH₂CH₂C(CF₃)₂O—, binaphtholate dianions, pinacolate dianions, —P(CH₃)₂(CH₂)₂P(CH₃)₂—, and —OC(CH₃)₂(CH₃)₂CO—. Preferred bidentate ligands are —P(Ph)₂CH₂CH₂P(Ph)₂- and —P(CH₃)₂(CH₂)₂P(CH₃)₂—. Tridentate ligands include, but are not limited to, (CH₃)₂NCH₂CH₂P(Ph)CH₂CH₂N(CH₃)₂. Other preferred tridentate ligands are those in which any three of X¹, X², L¹, L², L³, R¹, and R² (e.g., X¹, L¹, and L²) are taken together to be cyclopentadienyl, indenyl, or fluorenyl, each optionally substituted with C₂-C₂₀ alkenyl, C₂-C₂₀ alkynyl, C₁-C₂₀ alkyl, C₅-C₂₀ aryl, C₁-C₂₀ alkoxy, C₂-C₂₀ alkenyloxy, C₂-C₂₀ alkynyloxy, C₅-C₂₀ aryloxy, C₂-C₂₀ alkoxycarbonyl, C₁-C₂₀ alkylthio, C₁-C₂₀ alkylsulfonyl, or C₁-C₂₀ alkylsulfinyl, each of which may be further substituted with C₁-C₆ alkyl, halide, C₁-C₆ alkoxy or with a phenyl group optionally substituted with halide, C₁-C₆ alkyl, or C₁-C₆ alkoxy. More preferably, in compounds of this type, X, L¹, and L² are taken together to be cyclopentadienyl or indenyl, each optionally substituted with vinyl, C₁-C₁₀ alkyl, C₅-C₂₀ aryl, C₁-C₁₀ carboxylate, C₂-C₁₀ alkoxycarbonyl, C₁-C₁₀ alkoxy, or C₅-C₂₀ aryloxy, each optionally substituted with C₁-C₆ alkyl, halide, C₁-C₆ alkoxy or with a phenyl group optionally substituted with halide, C₁-C₆ alkyl or C₁-C₆ alkoxy. Most preferably, X, L¹ and L² may be taken together to be cyclopentadienyl, optionally substituted with vinyl, hydrogen, methyl, or phenyl. Tetradentate ligands include, but are not limited to O₂C(CH₂)₂P(Ph)(CH₂)₂P(Ph)(CH₂)₂CO₂, phthalocyanines, and porphyrins.

Complexes wherein L² and R² are linked are examples of the fourth group of catalysts, and are commonly called “Grubbs-Hoveyda” catalysts. Examples of Grubbs-Hoveyda-type catalysts include the following:

wherein L¹, X¹, X², and M are as described for any of the other groups of catalysts.

In addition to the catalysts that have the structure of formula (III), as described above, other transition metal carbene complexes include, but are not limited to:

neutral ruthenium or osmium metal carbene complexes containing metal centers that are formally in the +2 oxidation state, have an electron count of 16, are penta-coordinated, and are of the general formula (IX);

neutral ruthenium or osmium metal carbene complexes containing metal centers that are formally in the +2 oxidation state, have an electron count of 18, are hexa-coordinated, and are of the general formula (X);

cationic ruthenium or osmium metal carbene complexes containing metal centers that are formally in the +2 oxidation state, have an electron count of 14, are tetra-coordinated, and are of the general formula (XI); and

cationic ruthenium or osmium metal carbene complexes containing metal centers that are formally in the +2 oxidation state, have an electron count of 14, are tetra-coordinated, and are of the general formula (XII)

wherein: X¹, X², L¹, L², n, L³, R¹, and R² are as defined for any of the previously defined four groups of catalysts; r and s are independently zero or 1; t is an integer in the range of zero to 5;

Y is any non-coordinating anion (e.g., a halide ion, BF₄ ⁻, etc.); Z¹ and Z² are independently selected from —O—, —S—, —NR²—, —PR²—, —P(═O)R²—, —P(OR²)—, —P(═O)(OR²)—, —C(═O)—, —C(═O)O—, —OC(═O)—, —OC(═O)O—, —S(═O)—, and —S(═O)₂—; Z³ is any cationic moiety such as —P(R²)₃ ⁺ or —N(R²)₃ ⁺; and

any two or more of X¹, X², L¹, L², L³, n, Z¹, Z², Z³, R¹, and R² may be taken together to form a cyclic group, e.g., a multidentate ligand, and

wherein any one or more of X¹, X², L¹, L², n, L³, Z¹, Z², Z³, R¹, and R² may be attached to a support.

Other suitable complexes include Group 8 transition metal carbenes bearing a cationic substituent, such as are disclosed in U.S. Pat. No. 7,365,140 (Piers et al.) having the general structure (XIII):

wherein:

M is a Group 8 transition metal;

L¹ and L² are neutral electron donor ligands;

X¹ and X² are anionic ligands;

R¹ is hydrogen, C₁-C₁₂ hydrocarbyl, or substituted C₁-C₁₂ hydrocarbyl;

W is an optionally substituted and/or heteroatom-containing C₁-C₂₀ hydrocarbylene linkage;

Y is a positively charged Group 15 or Group 16 element substituted with hydrogen, C₁-C₁₂ hydrocarbyl, substituted C₁-C₁₂ hydrocarbyl; heteroatom-containing C₁-C₁₂ hydrocarbyl, or substituted heteroatom-containing hydrocarbyl;

Z⁻ is a negatively charged counterion;

m is zero or 1; and

n is zero or 1;

-   -   wherein any two or more of L¹, L², X¹, X², R¹, W, and Y can be         taken together to form a cyclic group.     -   Each of M, L¹, L², X¹, and X² in structure (XIII) may be as         previously defined herein.

W is an optionally substituted and/or heteroatom-containing C₁-C₂₀ hydrocarbylene linkage, typically an optionally substituted C₁-C₁₂ alkylene linkage, e.g., —(CH₂)_(i)— where i is an integer in the range of 1 to 12 inclusive and any of the hydrogen atoms may be replaced with a non-hydrogen substituent as described earlier herein with regard to the definition of the term “substituted.” The subscript n is zero or 1, meaning that W may or may not be present. In a preferred embodiment, n is zero.

Y is a positively charged Group 15 or Group 16 element substituted with hydrogen, C₁-C₁₂ hydrocarbyl, substituted C₁-C₁₂ hydrocarbyl, heteroatom-containing C₁-C₁₂ hydrocarbyl, or substituted heteroatom-containing hydrocarbyl. Preferably, Y is a C₁-C₁₂ hydrocarbyl-substituted, positively charged Group 15 or Group 16 element. Representative Y groups include P(R²)₃, P(R²)₃, As(R²)₃, S(R²)₂, O(R²)₂, where the R² are independently selected from C₁-C₁₂ hydrocarbyl; within these, preferred Y groups are phosphines of the structure P(R²)₃ wherein the R² are independently selected from C₁-C₁₂ alkyl and aryl, and thus include, for example, methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, t-butyl, cyclopentyl, cyclohexyl, and phenyl. Y can also be a heterocyclic group containing the positively charged Group 15 or Group 16 element. For instance, when the Group 15 or Group 16 element is nitrogen, Y may be an optionally substituted pyridinyl, pyrazinyl, or imidazolyl group.

Z⁻ is a negatively charged counterion associated with the cationic complex, and may be virtually any anion, so long as the anion is inert with respect to the components of the complex and the reactants and reagents used in the metathesis reaction catalyzed. Preferred Z⁻ moieties are weakly coordinating anions, such as, for instance, [B(C₆F₅)₄]⁻, [BF₄]⁻, [B(C₆H₆)₄]⁻, [CF₃S(O)₃]⁻, [PF₆]⁻, [SbF₆]⁻, [AlCl₄]⁻, [FSO₃]⁻, [CB₁₁H₆Cl₆]⁻, [CB₁₁H₆Br₆]⁻, and [SO₃F:SbF₅]⁻. Preferred anions suitable as Z⁻ are of the formula B(R¹⁵)₄ ⁻ where R¹⁵ is fluoro, aryl, or perfluorinated aryl, typically fluoro or perfluorinated aryl. Most preferred anions suitable as Z⁻ are BF₄ ⁻ and B(C₆F₅)⁻, optimally the latter.

It should be emphasized that any two or more of X¹, X², L¹, L², R¹, W, and Y can be taken together to form a cyclic group, as disclosed, for example, in U.S. Pat. No. 5,312,940 to Grubbs et al. When any of X¹, X², L¹, L², R¹, W, and Y are linked to form cyclic groups, those cyclic groups may be five- or six-membered rings, or may comprise two or three five- or six-membered rings, which may be either fused or linked. The cyclic groups may be aliphatic or aromatic, and may be heteroatom-containing and/or substituted, as explained in part (I) of this section.

One group of exemplary catalysts encompassed by the structure of formula (XIII) are those wherein m and n are zero, such that the complex has the structure of formula (XIV)

Possible and preferred X¹, X², and L¹ ligands are as described earlier with respect to complexes of formula (I), as are possible and preferred Y⁺ and Z⁻ moieties. M is Ru or Os, preferably Ru, and R¹ is hydrogen or C₁-C₁₂ alkyl, preferably hydrogen.

In formula (XIV)-type catalysts, L¹ is preferably a heteroatom-containing carbene ligand having the structure of formula (XV)

such that complex (XIV) has the structure of formula (XVI)

wherein X¹, X², R¹, R², Y, and Z are as defined previously, and the remaining substituents are as follows:

Z¹ and Z² are heteroatoms typically selected from N, O, S, and P. Since O and S are divalent, j is necessarily zero when Z¹ is O or S, and k is necessarily zero when Z² is O or S. However, when Z¹ is N or P, then j is 1, and when Z² is N or P, then k is 1. In a preferred embodiment, both Z¹ and Z² are N.

Q¹, Q², Q³, and Q⁴ are linkers, e.g., C₁-C₁₂ hydrocarbylene, substituted C₁-C₁₂ hydrocarbylene, heteroatom-containing C₁-C₁₂ hydrocarbylene, substituted heteroatom-containing C₁-C₁₂ hydrocarbylene, or —(CO)—, and w, x, y, and z are independently zero or 1, meaning that each linker is optional. Preferably, w, x, y, and z are all zero.

R³, R^(3A), R⁴, and R^(4A) are independently selected from hydrogen, hydrogen, C₁-C₂₀ hydrocarbyl, substituted C₁-C₂₀ hydrocarbyl, heteroatom-containing C₁-C₂₀ hydrocarbyl, and substituted heteroatom-containing C₁-C₂₀ hydrocarbyl.

Preferably, w, x, y, and z are zero, Z¹ and Z¹ are N, and R^(3A) and R^(4A) are linked to form -Q-, such that the complex has the structure of formula (XVII)

wherein R³ and R⁴ are defined above, with preferably at least one of R³ and R⁴, and more preferably both R³ and R⁴, being alicyclic or aromatic of one to about five rings, and optionally containing one or more heteroatoms and/or substituents. Q is a linker, typically a hydrocarbylene linker, including C₁-C₁₂ hydrocarbylene, substituted C₁-C₁₂ hydrocarbylene, heteroatom-containing C₁-C₁₂ hydrocarbylene, or substituted heteroatom-containing C₁-C₁₂ hydrocarbylene linker, wherein two or more substituents on adjacent atoms within Q may be linked to form an additional cyclic structure, which may be similarly substituted to provide a fused polycyclic structure of two to about five cyclic groups. Q is often, although not necessarily, a two-atom linkage or a three-atom linkage, e.g., —CH₂—CH₂—, —CH(Ph)-CH(Ph)- where Ph is phenyl; ═CR—N═, giving rise to an unsubstituted (when R═H) or substituted (R=other than H) triazolyl group; or —CH₂—SiR₂—CH₂— (where R is H, alkyl, alkoxy, etc.).

In a more preferred embodiment, Q is a two-atom linkage having the structure —CR⁸R⁹—CR¹⁰R¹¹— or —CR═CR¹⁰—, preferably —CR⁸R⁹—CR¹⁰R¹¹—, wherein R⁸, R⁹, R¹⁰, and R¹¹ are independently selected from hydrogen, C₁-C₁₂ hydrocarbyl, substituted C₁-C₁₂ hydrocarbyl, heteroatom-containing C₁-C₁₂ hydrocarbyl, substituted heteroatom-containing C₁-C₁₂ hydrocarbyl, and functional groups as defined in part (I) of this section. Examples of functional groups here include carboxyl, C₁-C₂₀ alkoxy, C₅-C₂₀ aryloxy, C₂-C₂₀ alkoxycarbonyl, C₂-C₂₀ alkoxycarbonyl, C₂-C₂₀ acyloxy, C₁-C₂₀ alkylthio, C₅-C₂₀ arylthio, C₁-C₂₀ alkylsulfonyl, and C₁-C₂₀ alkylsulfinyl, optionally substituted with one or more moieties selected from C₁-C₁₀ alkyl, C₁-C₁₀ alkoxy, C₅-C₂₀ aryl, hydroxyl, sulfhydryl, formyl, and halide. Alternatively, any two of R⁸, R⁹, R¹⁰, and R¹¹ may be linked together to form a substituted or unsubstituted, saturated or unsaturated ring structure, e.g., a C₄-C₁₂ alicyclic group or a C₅ or C₆ aryl group, which may itself be substituted, e.g., with linked or fused alicyclic or aromatic groups, or with other substituents.

Further details concerning such formula (XIII) complexes, as well as associated preparation methods, may be obtained from U.S. Pat. No. 7,365,140, herein incorporated by reference.

As is understood in the field of catalysis, suitable solid supports for any of the catalysts described herein may be of synthetic, semi-synthetic, or naturally occurring materials, which may be organic or inorganic, e.g., polymeric, ceramic, or metallic. Attachment to the support will generally, although not necessarily, be covalent, and the covalent linkage may be direct or indirect, if indirect, typically through a functional group on a support surface.

Non-limiting examples that may be used in the reactions of the disclosure include the following, some of which for convenience are identified throughout this disclosure by reference to their molecular weight:

In the foregoing molecular structures and formulae, Ph represents phenyl, Cy represents cyclohexane, Me represents methyl, nBu represents n-butyl, i-Pr represents isopropyl, py represents pyridine (coordinated through the N atom), and Mes represents mesityl (i.e., 2,4,6-trimethylphenyl).

Further examples of catalysts useful in the reactions of the present disclosure include the following: ruthenium (II) dichloro (3-methyl-1,2-butenylidene)bis(tricyclopentylphosphine) (C716); ruthenium (II) dichloro (3-methyl-1,2-butenylidene)bis(tricyclohexylphosphine) (C801); ruthenium (II) dichloro (phenylmethylene)bis(tricyclohexylphosphine) (C823); ruthenium (II) [1,3-bis-(2,4,6-trimethylphenyl)-2-imidazolidinylidene)dichloro (phenylmethylene) (triphenylphosphine) (C830), and ruthenium (II) dichloro (vinyl phenylmethylene)bis(tricyclohexylphosphine) (C835); ruthenium (II) dichloro (tricyclohexylphosphine) (o-isopropoxyphenylmethylene) (C601), and ruthenium (II) (1,3-bis-(2,4,6,-trimethylphenyl)-2-imidazolidinylidene)dichloro (phenylmethylene) (bis 3-bromopyridine (C884)).

Exemplary ruthenium-based metathesis catalysts include those represented by structures 12 (commonly known as Grubbs's catalyst), 14 and 16. Structures 18, 20, 22, 24, 26, 28, 60, 62, 64, 66, and 68 represent additional ruthenium-based metathesis catalysts. Catalysts C627, C682, C697, C712, and C827 represent still additional ruthenium-based catalysts. General structures 50 and 52 represent additional ruthenium-based metathesis catalysts of the type reported in Chemical & Engineering News; Feb. 12, 2007, at pages 37-47. In the structures, Ph is phenyl, Mes is mesityl, py is pyridine, Cp is cyclopentyl, and Cy is cyclohexyl.

Techniques for using the metathesis catalysts are known in the art (see, for example, U.S. Pat. Nos. 7,102,047; 6,794,534; 6,696,597; 6,414,097; 6,306,988; 5,922,863; 5,750,815; and metathesis catalysts with ligands in U.S. Publication No. 2007/0004917 A1), all incorporated by reference herein in their entireties. A number of the metathesis catalysts as shown are manufactured by Materia, Inc. (Pasadena, Calif.).

Additional exemplary metathesis catalysts include, without limitation, metal carbene complexes selected from the group consisting of molybdenum, osmium, chromium, rhenium, and tungsten. The term “complex” refers to a metal atom, such as a transition metal atom, with at least one ligand or complexing agent coordinated or bound thereto. Such a ligand typically is a Lewis base in metal carbene complexes useful for alkene, alkyne or alkene-metathesis. Typical examples of such ligands include phosphines, halides and stabilized carbenes. Some metathesis catalysts may employ plural metals or metal co-catalysts (e.g. a catalyst comprising a tungsten halide, a tetraalkyl tin compound, and an organoaluminum compound).

An immobilized catalyst can be used for the metathesis process. An immobilized catalyst is a system comprising a catalyst and a support, the catalyst associated with the support. Exemplary associations between the catalyst and the support may occur by way of chemical bonds or weak interactions (e.g. hydrogen bonds, donor acceptor interactions) between the catalyst, or any portions thereof, and the support or any portions thereof. Support is intended to include any material suitable to support the catalyst. Typically, immobilized catalysts are solid phase catalysts that act on liquid or gas phase reactants and products. Exemplary supports are polymers, silica, or alumina. Such an immobilized catalyst may be used in a flow process. An immobilized catalyst can simplify purification of products and recovery of the catalyst so that recycling the catalyst may be more convenient.

The metathesis process for producing industrial chemicals can be conducted under any conditions adequate to produce the desired metathesis product or products. For example, stoichiometry, atmosphere, solvent, temperature and pressure can be selected to produce a desired product and to minimize undesirable byproducts. The metathesis process may be conducted under an inert atmosphere. Similarly, if an olefin reagent is supplied as a gas, an inert gaseous diluent can be used. The inert atmosphere or inert gaseous diluent typically is an inert gas, meaning that the gas does not interact with the metathesis catalyst to substantially impede catalysis. For example, particular inert gases are selected from the group consisting of helium, neon, argon, nitrogen, and combinations thereof.

Similarly, if a solvent is used, the solvent chosen may be selected to be substantially inert with respect to the metathesis catalyst. For example, substantially inert solvents include, without limitation, aromatic hydrocarbons, such as benzene, toluene, xylenes, etc.; halogenated aromatic hydrocarbons, such as chlorobenzene and dichlorobenzene; aliphatic solvents, including pentane, hexane, heptane, cyclohexane, etc.; and chlorinated alkanes, such as dichloromethane, chloroform, dichloroethane, etc.

In certain embodiments, a ligand may be added to the metathesis reaction mixture. In many embodiments using a ligand, the ligand is selected to be a molecule that stabilizes the catalyst, and may thus provide an increased turnover number for the catalyst. In some cases the ligand can alter reaction selectivity and product distribution. Examples of ligands that can be used include Lewis base ligands, such as, without limitation, trialkylphosphines, for example tricyclohexylphosphine and tributyl phosphine; triarylphosphines, such as triphenylphosphine; diarylalkylphosphines, such as, diphenylcyclohexylphosphine; pyridines, such as 2,6-dimethylpyridine, 2,4,6-trimethylpyridine; as well as other Lewis basic ligands, such as phosphine oxides and phosphinites. Additives may also be present during metathesis that increase catalyst lifetime.

Using currently known catalysts, the metathesis processing temperature may largely be a rate-dependent variable where the temperature is selected to provide a desired product at an acceptable production rate. The selected temperature may be greater than about −40° C., may be more than about −20° C., and is generally selected to be more than about 0° C. or more than about 20° C. Generally, the process temperature may be no more than about 150° C., and may be no more than about 120° C. Thus, an exemplary temperature range for the metathesis reaction may be from about 20° C. to about 120° C. Lower temperatures can be used, for example, to minimize the production of undesired impurities or to favor a particular reaction pathway.

Any useful amount of the selected metathesis catalyst can be used in the process. For example, the molar ratio of the unsaturated polyol ester to catalyst may range from about 5:1 to about 10,000,000:1 or from about 50:1 to 500,000:1.

The metathesis process steps (i.e., step (b) and step (d)) can be conducted under any desired pressure. For example, the cross-metathesis step (b) is typically conducted at a pressure ranging from about 10 kPa to about 7000 kPa or from about 100 kPa to about 3000 kPa. In some embodiments, it is preferred to conduct the self-metathesis step (i.e., step (d)) at low pressure, for example, about 0.01 kPa to about 100 kPa, more typically about 0.01 kPa to about 50 kPa. By conducting the self-metathesis at low pressure, the low boiling point olefin products (e.g., the short-chain internal olefin or alpha olefin) that are formed during the cross-metathesis reaction can be easily separated from the higher boiling point functionalized olefin products (e.g., the one or more diacid olefins, diester olefins, or disalt olefins). This separation is advantageous for two reasons. First, in an integrated process, the separation of the short-chain internal olefin product allows this material to be recycled back to the reactor where the cross-metathesis step (i.e., step (b)) is being conducted. Second, the removal of the olefin products from the functionalized olefin products drives the equilibrium of the self-metathesis reaction (i.e., step (d)) to the formation of more functionalized olefin product. This results in a higher yield of the desired functionalized olefin product.

The metathesis reaction may be catalyzed by a system containing both a transition and a non-transition metal component. The most active and largest number of two-part catalyst systems are derived from Group VI A transition metals, for example, tungsten and molybdenum.

Separation Step (Step (c)):

After cross-metathesis with a short-chain olefin, at least a portion of the acid-, ester-, or carboxylate salt-functionalized alkene is separated from the remaining cross-metathesis products. If cross-metathesis is conducted on an unsaturated glyceride starting composition the resulting cross-metathesis products should be transesterified prior to separation. This allows the separation step to separate the ester-functionalized alkene from any ester functionalized alkane that may be present in the transesterification products.

Useful techniques for separating the acid-, ester-, or carboxylate salt-functionalized alkene from the remaining cross-metathesis products include, for example, distillation, reactive distillation, chromatography, fractional crystallization, membrane separation, liquid/liquid extraction, or a combination thereof.

In many embodiments, the acid-, ester-, or carboxylate salt-functionalized alkene can be purified to a high degree using one or more of the above-described techniques. For example, the acid-, ester-, or carboxylate salt-functionalized alkene can be purified to a level of 90% wt. or greater (e.g., 95% wt. or greater, 96% wt. or greater, 97% wt. or greater, 98% wt. or greater, 99% wt. or greater, 99.5% wt. or greater, or 99.9% wt. or greater). Using the method of the invention, a high purity functionalized alkene intermediate can be obtained using one or more conventional separation processes. Achieving a high purity functionalized alkene intermediate allows for the production of a high purity products from the methods of the invention For example, in some embodiments, the product has a purity of 90% wt. or greater (e.g., 95% wt. or greater, 96% wt. or greater, 97% wt. or greater, 98% wt. or greater, 99% wt. or greater, 99.5% wt. or greater, or 99.9% wt. or greater).

Self or Cross-Metathesis Step (Step (d)):

In some embodiments, after separation, the isolated acid-, ester-, or salt-functionalized alkene is self-metathesized in the presence of a metathesis catalyst to form a composition comprising one or more diacid alkenes, diester alkenes, or dicarboxylate salt alkenes. For example, when a Δ9 acid-functionalized starting composition is used and is cross-metathesized with 2-butene, the resulting acid-functionalized alkene has the structure HOOC—(CH₂)₇—CH═CH—CH₃. After separation, self-metathesis of the acid-functionalized alkene yields an unsaturated C18 diacid and 2-butene according to the formula below: 2 HOOC—(CH₂)₇—CH═CH—CH₃→HOOC—(CH₂)₇—CH═CH—(CH₂)₇—COOH+CH₃—CH═CH—CH₃

In similar fashion, when a Δ9 methyl ester-functionalized starting composition is used and is cross-metathesized with 2-butene, the resulting methyl ester-functionalized alkene has structure CH₃OOC—(CH₂)₇—CH═CH—CH₃. Self-metathesis of the ester-functionalized olefin yields an unsaturated C18 diester and 2-butene according to the formula below: 2CH₃OOC—(CH₂)₇—CH═CH—CH₃→CH₃OOC—(CH₂)₇—CH═CH—(CH₂)₇—COOCH₃+CH₃—CH═CH—CH₃

In another embodiment, a Δ5 acid-functionalized starting composition is used and is cross-metathesized with 2-butene to provide an acid-functionalized alkene having the structure HOOC—(CH₂)₃—CH═CH—CH₃. Self-metathesis of the acid-functionalized alkene yields an unsaturated C10 diacid and 2-butene according to the formula below: 2HOOC—(CH₂)₃—CH═CH—CH₃→HOOC—(CH₂)₃—CH═CH—(CH₂)₃—COOH+CH₃—CH═CH—CH₃

In another embodiment, a Δ6 acid-functionalized starting composition is used and is cross-metathesized with 2-butene to provide an acid-functionalized alkene having the structure HOOC—(CH₂)₄—CH═CH—CH₃. Self-metathesis of the ester-functionalized alkene yields an unsaturated C12 diacid and 2-butene according to the formula below: 2HOOC—(CH₂)₄—CH═CH—CH₃→HOOC—(CH₂)₄—CH═CH—(CH₂)₄—COOH+CH₃—CH═CH—CH₃

In another embodiment, a Δ13 acid-functionalized starting composition is used and is cross-metathesized with 2-butene to provide an acid-functionalized alkene having the structure HOOC—(CH₂)₁₁—CH═CH—CH₃. Self-metathesis of the ester-functionalized alkene yields an unsaturated C26 diacid and 2-butene according to the formula below: 2HOOC—(CH₂)₁₁—CH═CH—CH₃→HOOC—(CH₂)₁₁—CH═CH—(CH₂)₁₁—COOH+CH₃—CH═CH—CH₃

Other self-metathesis reactions would follow the above reaction scheme.

In some embodiments, after separation, the isolated acid-, ester-, or carboxylate salt-functionalized alkene is cross-metathesized with a second functionalized alkene compound in the presence of a metathesis catalyst to form a bifunctional organic compound. Exemplary bifunctional organic compounds obtainable by this method include diacids, acid/esters, acid/amines, acid/alcohols, acid/aldehydes, acid/ketones, acid/halides, acid/nitriles, as well as diesters, ester/amines, ester/alcohols, ester/aldehydes, ester/ketones, ester/halides, and ester/nitriles. In many embodiments, after cross-metathesis, the resulting bifunctional organic compound is hydrogenated in order to saturate the double-bond that is present in the bifunctional compound. For example, starting with fatty acids □5 and higher, alpha, omega-diacids from C7 to C18 and higher can be made. Similarly, omega-hydroxycarboxylic acids and omega-aminocarboxylic acids from C7 to C18 and higher can be made.

The second functionalized alkene compound has at least one carbon-carbon double bond and has at least one organic functional group. Examples of organic functional groups include carboxylic acids, esters, amines, amides, halogens, aldehydes, nitriles, isocyanates, ketones, epoxides, and alcohols. In many embodiments, the second functionalized alkene has the general structure: R¹²—CH═CH—(CH₂)_(n)—R¹³

where

-   -   n is 0 or an integer (typically 1 to 20);     -   —R¹² is hydrogen, an alkyl group, an aryl group, or         —(CH₂)_(n)—R¹³;     -   —R¹³ is a functional group (typically —COOH, —COOR¹⁴, —COH;         —COR¹⁴; —CONH₂; —C≡N; —NH₂; —OH; or —X);     -   —R¹⁴ is alkyl group or an aryl group; and     -   —X is a halogen (typically Cl, F, Br, or I).

Examples of second functionalized alkene compounds include 2-butene-1,4-dioic acid (HOOCCH═CHCOOH), acrylic acid (CH═CHCOOH), 2-butenoic acid (CH₃CH═CHCOOH), 2-pentenoic acid (CH₃CH₂CH═CHCOOH), 2-hexenoic acid (CH₃CH₂CH₂CH═CHCOOH), 3-hexenedioc acid (HOOCCH₂CH═CHCH₂COOH), the dimethyl ester of 3-hexenedioc acid (CH₃OOCCH₂CH═CHCH₂COOCH₃), 3-hexenoic acid (HOOCCH₂CH═CHCH₂CH₃), the methyl ester of 3-hexenoic acid (CH₃OOCCH₂CH═CHCH₂CH₃), 3-pentenoic acid (HOOCCH₂CH═CHCH₃), methyl ester of 3-pentenoic acid (CH₃OOCCH₂CH═CHCH₃), 4-pentenoic acid, 4-hexenoic acid, 4-heptenoic acid, 4-octenoic acid and its esters, 4-octene-1,8-dioic acid and its esters, 5-hexenoic acid, 1-bromo-3 hexene, 3-butenal diethyl acetal, 5-heptenoic acid, 5-octenoic acid and its esters, 5-decene-1,10-dioic acid and its esters, 6-heptenoic acid, 6-octenoic acid, 6-nonenoic acid, 6-decenoic acid and its esters, 6-dodecene-1,12-dioic acid and its esters, 7-octenoic acid, 7-nonenoic acid, 7-decenoic acid, 7-undecenoic acid, and 7-dodecenoic acid and its esters.

Additional examples of second functionalized alkene compounds include allyl alcohol, 2-butenol, 3-buten-1-ol, 2-penten-1-ol, 3-penten-1-ol, 4-penten-1-ol, 2-hexen-1-ol, 3-hexen-1-ol, 4-hexen-1-ol, 5-hexen-1-ol, and the like; buten-1,4-diol, 2-penten-1,5-diol, 2-hexen-1,6-diol, 3-hexen-1,6-diol, and the like; allyl amine, 1-amino-2-butene, 1-amino-3-butene, 1-amino-2-pentene, 1-amino-3-pentene, 1-amino-4-pentene, 1-amino-2-hexene, 1-amino-3-hexene, 1-amino-4 hexene, 1-amino-5-hexene, and the like; 1,4-diamino-2-butene, 1,5-diamino-2-pentene, 1,6-diamino-2-hexene, 1,6-diamino-3-hexene, and the like; 1-chloro-2-propene (i.e., allyl chloride), 1-chloro-2-butene, 1-chloro-3-butene, 1-chloro-2-pentene, 1-chloro-3-pentene, 1-chloro-4-pentene, 1-chloro-2-hexene, 1-chloro-3-hexene, 1-chloro-4-hexene, 1-chloro-5-hexene, and the like (including the F, Br, or I analogs); 1,4-dichloro-2-butene (Cl—CH₂—CH═CH—CH₂—Cl), 1,5-dichloro-2-pentene, 1,6-dichloro-2-hexene, 1,6-dichloro-3-hexene, and the like (including the F, Br, or I analogs); acrolein (propenal), 2-butenal, 3-butenal, 2-pentenal, 3-pentenal, 4-pentenal, 2-hexenal, 3-hexenal, 4-hexenal, 5-hexenal, and the like; 2-buten-1,4-dial, 2-penten-1,5-dial, 2-hexen-1,6-dial, 3-hexen-1,6-dial, and the like; acrylonitrile (cyanoethylene), 1-cyano-1-propene, 1-cyano-2-propene, 1-cyano-1-butene, 1-cyano-2-butene, 1-cyano-3-butene, 1-cyano-1-pentene, 1-cyano-2-pentene, 1-cyano-3-pentene, and the like; 1,2-dicyanoethylene, 1,3-dicyanopropene, 1,4-dicyano-1-butene, 1,4-dicyano-2-butene, and the like.

In exemplary embodiments, the second functionalized alkene is symmetric about its carbon-carbon double bond. That is, the group —R¹² is the same as group —(CH₂)_(n)—R¹³. Advantageously, when the second functionalized alkene is symmetric, the number of products formed in the cross-metathesis reaction is reduced as compared to cross-metathesis reactions where the second functionalized alkene is asymmetric. This may provide for higher yields and/or easier separation of the desired bifunctional compound. Representative examples of symmetric functionalized alkenes include maleic acid (HO₂CCH═CHCO₂H) and esters thereof, 3-hexenedioc acid (HO₂CCH₂CH═CHCH₂CO₂H) and esters thereof (e.g., the dimethyl ester of 3-hexenedioc acid (CH₃O₂CCH₂CH═CHCH₂CO₂CH₃)), 4-octene-1,8-dioic acid and esters thereof, 5-decene-1,10-dioic acid and esters thereof, and 6-dodecene-1,12-dioic acid esters.

In an exemplary embodiment, a Δ9 acid-functionalized starting composition is used and is cross-metathesized with 2-butene, providing an acid-functionalized alkene having the structure HO₂C—(CH₂)₇—CH═CH—CH₃. After separation, the acid-functionalized alkene is cross-metathesized with 3-hexenedioc acid (HO₂CCH₂CH═CHCH₂CO₂H) in the presence of a metathesis catalyst. The cross-metathesis yields an unsaturated C12 diacid according to the formula below: HO₂C—(CH₂)₇—CH═CH—CH₃+HO₂CCH₂CH═CHCH₂CO₂H→HO₂C—(CH₂)₇—CH═CH—CH₂—CO₂H+CH₃—CH═CHCH₂CO₂H

Optionally, the unsaturated C12 diacid may be hydrogenated to produce the corresponding saturated C12 diacid.

In another exemplary embodiment, a Δ9 acid-functionalized starting composition is used and is cross-metathesized with 2-butene, providing an acid-functionalized alkene having the structure HO₂C—(CH₂)₇—CH═CH—CH₃. After separation, the acid-functionalized alkene is cross-metathesized with maleic acid (HO₂C—CH═CH—CO₂H) in the presence of a metathesis catalyst. The cross-metathesis yields an unsaturated C11 diacid according to the formula below: HO₂C—(CH₂)₇—CH═CH—CH₃+HO₂C—CH═CH—CO₂H→HO₂C—(CH₂)₇—CH═CH—CO₂H+CH₃—CH═CH—CO₂H

Other examples of bifunctional organic products that may be made using the method of the invention are summarized in TABLES C-D.

TABLE C Second Starting Functionalized Composition Alkene Bifunctional Organic Compound Δ9 But-2-ene-1,4-dial 11-oxoundec-9-enoic acid acid OHCCH═CH(CH₂)₇CO₂H Δ9 But-2-ene-1,4- 10-carboxamidodec-9-enoic acid acid diamide H₂NCOCH═CH(CH₂)₇CO₂H Δ9 But-2-ene-1,4-diol 11-hydroxyundec-9-enoic acid acid HOCH₂CH═CH(CH₂)₇CO₂H Δ9 But-2-ene-1,4- 11-aminoundec-9-enoic acid acid diamine H₂NCH₂CH═CH(CH₂)₇CO₂H Δ9 But-2-ene-1,4- 11-chloroundec-9-enoic acid acid dichloride ClCH₂CH═CH(CH₂)₇CO₂H Δ9 Hex-3-ene-1,6-dial 12-oxododec-9-enoic acid acid OHCCH₂CH═CH(CH₂)₇CO₂H Δ9 Hex-3-ene-1,6- 11-carboxamidoundec-9-enoic acid diamide acid H₂NCOCH₂CH═CH(CH₂)₇CO₂H Δ9 Hex-3-ene-1,6-diol 12-hydroxydodec-9-enoic acid acid HO(CH₂)₂CH═CH(CH₂)₇CO₂H Δ9 Hex-3-ene-1,6- 12-aminododec-9-enoic acid acid diamine H₂N(CH₂)₂CH═CH(CH₂)₇CO₂H Δ9 Hex-3-ene-1,6- 12-chlorododec-9-enoic acid (or acid dichloride (or other other halogens) halogens) Cl(CH₂)₂CH═CH(CH₂)₇CO₂H

TABLE D Second Starting Functionalized Composition Alkene Bifunctional Organic Compound Δ9 methyl But-2-ene-1,4-dial Methyl 11-oxoundec-9-enoate ester OHCCH═CH(CH₂)₇CO₂CH₃ Δ9 methyl But-2-ene-1,4- Methyl 10-carboxamidodec-9- ester diamide enoate H₂NCOCH═CH(CH₂)₇CO₂CH₃ Δ9 methyl But-2-ene-1,4-diol Methyl 11-hydroxyundec-9- ester enoate HOCH₂CH═CH(CH₂)₇CO₂CH₃ Δ9 methyl But-2-ene-1,4- Methyl 11-aminoundec-9-enoate ester diamine H₂NCH₂CH═CH(CH₂)₇CO₂CH₃ Δ9 methyl But-2-ene-1,4- Methyl 11-chloroundec-9-enoate ester dichloride ClCH₂CH═CH(CH₂)₇CO₂CH₃ Δ9 methyl Hex-3-ene-1,6-dial Methyl 12-oxododec-9-enoate ester OHCCH₂CH═CH(CH₂)₇CO₂CH₃ Δ9 methyl Hex-3-ene-1,6- Methyl 11-carboxamidoundec-9- ester diamide enoate H₂NCH₂COCH═CH(CH₂)₇CO₂CH₃ Δ9 methyl Hex-3-ene-1,6-diol Methyl 12-hydroxydodec-9- ester enoate HO(CH₂)₂CH═CH(CH₂)₇CO₂CH₃ Δ9 methyl Hex-3-ene-1,6- Methyl 12-aminododec-9-enoate ester diamine H₂N(CH₂)₂CH═CH(CH₂)₇CO₂CH₃ Δ9 methyl Hex-3-ene-1,6- Methyl 12-chlorododec-9-enoate ester dichloride (or other (or other halogens) halogens) Cl(CH₂)₂CH═CH(CH₂)₇CO₂CH₃

Optionally, the above-listed unsaturated compounds may be hydrogenated to form the corresponding saturated compounds.

In some embodiments, where the bifunctional organic compound is a dicarboxylate ester alkene, an ester group of the dicarboxylate ester alkene is hydrolyzed to form a carboxylic acid group.

Hydrogenation Catalysts

After self- or cross-metathesis (i.e., step (d)), the resulting alkene may be hydrogenated to remove the carbon-carbon double bond. Hydrogenation is typically conducted by exposing the alkene to H₂ gas in the presence of a hydrogenation catalyst.

The principal component of the catalyst useful for the hydrogenation is selected from metals from the group consisting of palladium, ruthenium, rhenium, rhodium, iridium, platinum, nickel, cobalt, copper, iron, osmium; compounds thereof; and combinations thereof.

The catalyst may be supported or unsupported. A supported catalyst is one in which the active catalyst agent is deposited on a support material by a number of methods, such as spraying, soaking or physical mixing, followed by drying, calcination, and if necessary, activation through methods such as reduction or oxidation. Materials frequently used as a support are porous solids with high total surface areas (external and internal), which can provide high concentrations of active sites per unit weight of catalyst. The catalyst support may enhance the function of the catalyst agent. A supported metal catalyst is a supported catalyst in which the catalyst agent is a metal.

A catalyst that is not supported on a catalyst support material is an unsupported catalyst. An unsupported catalyst may be platinum black or a Raney™ (W.R. Grace & Co., Columbia, Md.) catalyst. Raney™ catalysts have a high surface area due to selectively leaching an alloy containing the active metal(s) and a leachable metal (usually aluminum). Raney® catalysts have high activity due to the higher specific area and allow the use of lower temperatures in hydrogenation reactions. The active metals of Raney™ catalysts include nickel, copper, cobalt, iron, rhodium, ruthenium, rhenium, osmium, iridium, platinum, palladium; compounds thereof; and combinations thereof.

The catalyst support useful herein can be any solid, inert substance including, but not limited to, oxides such as silica, alumina and titania; barium sulfate; calcium carbonate; and carbons. The catalyst support can be in the form of powder, granules, pellets, or the like.

A preferred support material of the invention is selected from the group consisting of carbon, alumina, silica, silica-alumina, silica-titania, titania, titania-alumina, barium sulfate, calcium carbonate, strontium carbonate, compounds thereof and combinations thereof. Supported metal catalysts can also have supporting materials made from one or more compounds. More preferred supports are carbon, titania and alumina. Further preferred supports are carbons with a surface area greater than 100 m²/g. A further preferred support is carbon with a surface area greater than 200 m²/g. Preferably, the carbon has an ash content that is less than 5% by weight of the catalyst support; the ash content is the inorganic residue (expressed as a percentage of the original weight of the carbon) which remains after incineration of the carbon.

The preferred content of the metal catalyst in the supported catalyst is from about 0.1% to about 20% of the supported catalyst based on metal catalyst weight plus the support weight. A more preferred metal catalyst content range is from about 1% to about 10% of the supported catalyst.

Combinations of metal catalyst and support system may include any one of the metals referred to herein with any of the supports referred to herein. Preferred combinations of metal catalyst and support include palladium on carbon, palladium on calcium carbonate, palladium on barium sulfate, palladium on alumina, palladium on titania, platinum on carbon, platinum on alumina, platinum on silica, iridium on silica, iridium on carbon, iridium on alumina, rhodium on carbon, rhodium on silica, rhodium on alumina, nickel on carbon, nickel on alumina, nickel on silica, rhenium on carbon, rhenium on silica, rhenium on alumina, ruthenium on carbon, ruthenium on alumina and ruthenium on silica.

Further preferred combinations of metal catalyst and support include palladium on carbon, palladium on alumina, palladium on titania, platinum on carbon, platinum on alumina, rhodium on carbon, rhodium on alumina, ruthenium on carbon and ruthenium on alumina.

The method of the invention will now be described with reference to FIG. 1 to FIG. 3. Referring now to FIG. 1, a process flow diagram of an embodiment of the method 10 of the invention is shown. In the method 10, starting material composition 12 is provided that comprises a Δ9 unsaturated fatty acid, a Δ9 unsaturated fatty ester, a salt thereof, or a mixture thereof. In reaction 14, starting material composition 12 is cross-metathesized with a short-chain internal olefin 16 in the presence of a first metathesis catalyst 17 to produce cross-metathesis products 18 comprising (i) one or more olefins 20, and (ii) one or more acid-, ester-, or salt-functionalized alkenes 22. Following this, at least a portion of the acid-, ester-, or salt-functionalized alkene 22 is separated 23 from the remaining cross-metathesis products 18. Spent metathesis catalyst 17 may also be removed. In the next step, the isolated acid-, ester-, or salt-functionalized alkene 22 is then self-metathesized 24 in the presence of a second metathesis catalyst 28 to produce a C18 diacid, diester, or disalt alkene 30 and one or more olefin products 32. Optionally, the C18 diacid, diester, or disalt alkene can be hydrogenated to form a saturated C18 diacid, diester, or disalt compound.

If the starting material comprises a fatty ester in glyceride form, the glyceride may be converted (e.g., by transesterification) into free fatty esters prior to being cross-metathesized with the short-chain internal olefin, or the glyceride can be cross-metathesized with the short-chain internal olefin followed by conversion (e.g., by transesterification) into free fatty esters.

Referring now to FIG. 2, a process flow diagram of an embodiment of the method 100 of the invention is shown. In this embodiment, a fatty acid triglyceride starting material is converted into free fatty esters prior to cross-metathesizing the free fatty esters with a short-chain internal olefin. In a first step of the method, triglyceride 102 and alcohol 104 are trans-esterified 106 in the presence of trans-esterification catalyst 105. Trans-esterification reaction 106 converts triglyceride 102 into glycerol 108 and free fatty esters 110. Together, the glycerol 108 and free fatty acid esters 110 are referred to as trans-esterification products 115. After trans-esterification reaction 106, a separation 114 (e.g., water wash or distillation) is conducted on the trans-esterification products 115 in order to separate the glycerol 108 from the free fatty acid esters 110. Spent metathesis catalyst 105 may also be removed.

After separation, a cross-metathesis reaction 118 is conducted between the free fatty esters 110 and short-chain internal olefin 116. The cross-metathesis 118 is conducted in the presence of a metathesis catalyst 120 in order to form cross-metathesis products 122 comprising one or more olefins 124 and one or more ester-functionalized alkenes 126. Following this, at least a portion of the ester-functionalized alkenes 126 are separated 128 (e.g., using distillation) from the cross-metathesis products 122. The isolated ester-functionalized alkene 126 is then self-metathesized 129 in the presence of a second metathesis catalyst 130 to produce the self-metathesis products 132 comprising a diester alkene 134 and one or more olefin products 136.

Referring to FIG. 3, a process flow diagram of another embodiment of the method 200 of the invention is shown. In this embodiment, a fatty acid triglyceride starting material is cross-metathesized with a short-chain internal olefin. In the first reaction of method 200, triglyceride 202 and short-chain internal olefin 216 are cross-metathesized 218 in the presence of a metathesis catalyst 220 to form cross-metathesis products 222. Cross-metathesis products 222 comprise one or more olefins 224 and one or more ester-functionalized alkenes 225. In this embodiment, the ester-functionalized alkenes 225 are triglycerides. The cross-metathesis products 222 are then separated 228 into one or more ester-functionalized alkenes (triglyceride) products 225 and one or more olefins 224. Spent metathesis catalyst 220 can also be removed. Following this, the ester-functionalized alkene (triglyceride) products 225 are trans-esterified 206 with an alcohol 204 in the presence of a trans-esterification catalyst 205. Trans-esterification reaction 206 converts the ester-functionalized alkene (triglyceride) products 225 into trans-esterification products 215 comprising glycerol 208 and free ester-functionalized alkene 240. After trans-esterification reaction 206, a separation 214 is conducted in order to separate the glycerol 208 from the free ester-functionalized alkene 240. The free ester-functionalized alkene 240 is then self-metathesized 228 in the presence of a metathesis catalyst 230 in order to form a diester alkene product 234 and one or more olefin products 236. In an alternative embodiment (not shown in FIG. 3), the ester-functionalized alkene (triglyceride) is self-metathesized and the resulting product is trans-esterified to produce glycerol and free ester-functionalized alkene.

In an exemplary embodiment, as shown in FIG. 2A, triglyceride 102A is reacted with methanol 104A in trans-esterification reaction 106A in the presence of trans-esterification catalyst 105A. Trans-esterification reaction 106A converts triglyceride 102A into glycerol 108A and free fatty acid methyl esters 110A. Collectively, glycerol 108A and free fatty acid methyl esters 110A are referred to as trans-esterification products 115A. In this embodiment, the free fatty acid methyl esters 110A comprise methyl oleate (i.e., the methyl ester of oleic acid), methyl linoleate (i.e., the methyl ester of linoleic acid), and methyl linolenate (i.e., the methyl ester of linolenic acid). After trans-esterification reaction 106A, separation process 114A is conducted on the trans-esterification products 115A in order to separate the glycerol 108A from the free fatty acid methyl esters 110A. Spent metathesis catalyst 105A can also be removed. Following separation, the free fatty acid methyl esters 110A and 2-butene 116A (i.e., a short-chain internal olefin) are cross-metathesized 118A in the presence of a metathesis catalyst 120A to form cross-metathesis products 122A comprising olefins 124A and ester-functionalized alkenes 126A. The cross-metathesis products 122A are then separated by separation process 128A into product streams comprising 9-undecenoic acid methyl ester 125A, 2-undecene 127A, 2-octene 129A, 2,5-heptadiene 131A, and 2-pentene 133A. Next, 9-undecenoic acid methyl ester 125A is self-metathesized 140A in the presence of a metathesis catalyst 142A to form self-metathesis products 143A comprising a C18 diester alkene 144A and 2-butene 146A. Optionally, the C18 diester alkene 144A can be hydrogenated to form a saturated C18 diester 148A.

In another exemplary embodiment, as shown in FIG. 2B, triglyceride 102B is reacted with methanol 104B in trans-esterification reaction 106B in the presence of trans-esterification catalyst 105B. Trans-esterification reaction 106B converts triglyceride 102B into trans-esterification products 115B including glycerol 108B and free fatty acid methyl ester 110B. After trans-esterification reaction 106B, separation process 114B is conducted on the trans-esterification products 115B in order to separate the glycerol 108B from the free fatty acid methyl ester 110B. Spent metathesis catalyst 105B can also be removed. Following separation, fatty acid methyl ester 110B and 3-hexene 116B (i.e., a short-chain internal olefin) are cross-metathesized 118B in the presence of a metathesis catalyst 120B to form cross-metathesis products 122B comprising olefins 124B and ester-functionalized alkenes 126B. Cross-metathesis products 122B are separated via separation process 128B into product streams comprising: 9-dodecenoic acid methyl ester 125B, 3-dodecene 127B, 3-nonene 129B, 3,6-nonadiene 131B, and 3-hexene 133B. Next, 9-dodecenoic acid methyl ester 125B is self-metathesized 140B in the presence of a metathesis catalyst 142B to form self-metathesis products 143B comprising a C18 dimethyl ester alkene 144B and 3-hexene 146B. Optionally, the C18 diester alkene can be hydrogenated to form a saturated C18 dimethyl ester 148B.

The invention will now be described with reference to the following non-limiting examples.

EXAMPLES Example 1 Synthesis of 1,18-Diester (1,18-dimethyl ester of 9-octadecene) from 3-Hexene and Soybean Oil

Step 1: Production of Methyl 9-dodecenoate [CH₃CH₂CH═CH(CH₂)₇CO₂CH₃]

Metathesis reactions were conducted in a 250 ml 3-neck round bottom Schlenk flask that was equipped with a reflux condenser (connected to a bubbler), two septa, a stir bar, and a thermocouple. Prior to adding any reactants, the apparatus was degassed with argon for thirty minutes. Then, 70 ml (64.4 g) of degassed soybean oil (Cargill soybean oil (Salad oil), Lot # F4102) was added to the apparatus. In a separate container, 3-hexene was degassed with argon for one hour. Following degassing, 127 ml (86.4 grams) of the degassed 3-hexene was added to the flask using a graduated cylinder. The resulting mixture was degassed for fifteen minutes with argon. The mixture was then heated to 65° C. before adding the metathesis catalyst.

Metathesis catalyst (C827, Lot #067-050B) was added to the degassed mixture of soybean oil and 3-hexene in the amount shown in TABLE 1. In each case, the resulting mixture was allowed to react at 65° C., with aliquots taken at 2, 4, and 6 hours to check for conversion using a gas chromatograph. Maximum conversion was reached after two hours in all cases. In each case, after reacting for 6 hours, 1.30 grams of activated clay (Pure-Flo B80 natural Bleaching Adsorbent) was added, and the resulting composition was stirred overnight. Following this, the composition was filtered through a bed of silica to remove the activated clay and metathesis catalyst. The filtrates were sealed in a sample bottle and refrigerated. Percent yield of methyl 9-dodecenoate was determined using a gas chromatograph. The resulting data is presented in TABLE 1.

TABLE 1 Catalyst Loading¹ % Yield of Methyl 9- Example No. (ppm) dodecenoate² 1-1 100 33.7 1-2 75 40.1 1-3 50 30.5 1-4 100 33.0 ¹Catalyst 827 loading in ppm per double bond of SBO. 3-Hexene was added in 3 equivalents per double bond of SBO. ²GC yield after 2 hours, yields did not change significantly at 6 hours.

Step 2: Self-Metathesis of Methyl 9-Dodecenoate

Samples of methyl 9-dodecenoate were warmed to temperature (see, TABLE 2) and were degassed with argon for 30 minutes. Next, a metathesis catalyst (see, TABLE 2) was added to the methyl 9-dodecenoate and vacuum was applied to provide a pressure of <1 mmHg. The methyl 9-dodecenoate was then allowed to self-metathesize for the time reported in TABLE 2. GC analysis indicated that 1,18-dimethyl ester of 9-octadecene [CH₃O₂C(CH₂)₇CH═CH(CH₂)₇CO₂CH₃] was produced in the yield reported in TABLE 2.

TABLE 2 Catalyst Reaction Reaction Example Catalyst Loading Time Temp. 9-C18(O₂Me)₂ No. 9C₁₂O₂Me No. (ppm) (hours) (° C.) (GC Area %) 1-5 10.6 C-827 100 3 50 83.5 1-6 10.6 C-827 150 3 50 87.0 1-7 10.6 C-848 75 20 25 86.0 1-8 10.6 C-848 150 20 25 81.1 1-9 10.6 C-827 50 3 50 82.5 1-10 10.6 C-848 25 5 40 83.7 1-11 10.6 C-827 25 3 50 83.0 1-12 10.6 C-827 10 3 50 66.2 1-13 10.6 C-827 17 4 50 81.8 1-14 10.6 C-827 15 4 50 90.0 1-15 10.6 C-827 13 4 50 89.9 1-16 10.6 C-827 10 4 50 81.1 1-17 10.6 C-827 5 4 50 50.9 1-18 10.6 C-627 25 4 55 84.0 1-19 10.6 C-627 10 4 55 87.5

Example 2 Vacuum Distillation of 9C₁₂O₂Me

A glass 2.0 L 3-necked round bottom flask with a magnetic stirrer, packed 5 column, distillation head, and temperature controller was charged with esterified products and was placed in a heating mantle. The flask was attached to a 2-inch×36-inch glass distillation packed column containing 0.16″ Pro-Pak™ stainless steel saddles. The distillation column was connected to a fractional distillation head, which was connected to a vacuum line. A 500 mL pre-weighed round bottom flask was used to collect the distilled fractions. During distillation, vacuum was applied to provide a pressure of <1 mmHg. TABLE 3 contains the vacuum distillation results.

TABLE 3 Distillation Data Distillation Head Pot Isolated GC Retention Distillation Temperature Temperature Weight Time Fraction (° C.) (° C.) (grams) (min) 3C₉ + 3,6 C₉ 26 37 136.5 1.6 3C₁₂ + 3,6 C₁₂ 48 58 125.4 3.87 6C₁₅ + 6,9 C₁₅ 92-94 115-120 68 7.45 9C₁₂ − O₂Me 93-96 120-122 275.4 7.88

6C₁₅+6.9C₁₅ impurities were separated from 9C₁₂O₂Me by equilibrating the distillation column for 24 hours, followed by collecting 6C₁₅+6.9C₁₅ with a reflux ratio of 1:10 (i.e. 1 drop collected for every 10 drops sent back to the packed column). This procedure demonstrates that 9C₁₂O₂Me (275.4 g.) could be isolated in 50.9% yield and in 99.2% chemical purity. The 6C₁₅+6.9C₁₅ impurities could be removed by fractional distillation.

Example 3 Self-Metathesis of methyl 9-decenoate

Methyl 9-decenoate (25 g, 114 mmol, ˜90% chemical purity) obtained by ethenolysis of methyl oleate was charged in a 250 mL round-bottomed flask and was degassed with argon for 30 min. C823 metathesis catalyst (127 mg, 0.15 mmol, 0.13 mol %) was then added, and the reaction contents were heated to 35° C. under vacuum for 16 hrs. A 1.0 M solution of tris(hydroxymethyl)phosphine (4 mL) was then added and the reaction contents were heated to 90° C. for 4 hr. The reaction contents were then cooled to room temperature and were diluted with 50 mL of ethyl acetate. The diluted reaction contents were then washed sequentially with (1) 50 mL of 1.0 M aqueous HCl, (2) water, and (3) brine. The resulting organic phase was then dried with anhydrous sodium sulfate, filtered, and concentrated by rotary evaporation. 1 gram of the crude diester (1,18-dimethyl 9-octadecenedioate) was then dissolved in 4.5 mL of hexanes and the resulting homogeneous solution was cooled to −11° C. for 5 hrs. The crystals that formed were filtered and air-dried. GC analysis of the crystals indicated 95.8% chemical purity and 99:1 E:Z isomeric ratio.

Example 4 Preparation of 1,12-Diester of Dodecene from Methyl-9-Dodecenoate and Methyl-3-Pentenoate

Step 1: Methyl-9-Dodecenoate was prepared as described in Step 1 of EXAMPLE 1.

Step 2: Cross-metathesis of Methyl 9-dodecenoate with Methyl-3-Pentenoate

Methyl 9-dodecenoate and methyl-3-pentenoate were combined and degassed with argon for 30 minutes, then warmed to temperature (see, TABLE 4). Next, a metathesis catalyst (see, TABLE 4) was added to the methyl 9-dodecenoate and methyl-3-pentenoate mixture. The mixture was then allowed to metathesize for the time reported in TABLE 4. GC analysis indicated that 1,12-dimethyl ester of dodecene [CH₃O₂C(CH₂)₇CH═CH(CH₂)CO₂CH₃] was produced in the GC yield reported in TABLE 4.

TABLE 4

Equiv of catalyst GC Area % Example methyl- loading Temp Product No. 3-pentenoate catalyst (ppm) (° C.) 30 min 60 min 120 min 240 min 4-1 1 827 1000 60 ND ND ND 27.1 4-2 3 827 1000 60 ND ND ND 36.4 4-3 5 827 1000 60 ND ND ND 32.9 4-4 3 827 100 60 ND ND ND 2.5 4-5 3 827 250 60 ND ND ND 12.0 4-6 3 827 500 60 ND ND ND 28.9 4-7 3 827 250 50 ND ND ND 15.0 4-8 3 827 250 70 ND ND ND 9.8 4-9 3 827 100 60 0.0 0.0 0.0 0.0 4-10 3 827 50 60 0.0 0.0 0.0 0.0 4-11 3 827 25 60 0.0 0.0 0.0 0.0 *ND = no data ¹No conversion was seen at lower catalyst loadings.

Example 5 Preparation of Methyl 11-Chloro-9-undecenoate from Methyl-9-Dodecenoate and 1,4-Dichloro-2-butene

Step 1: Methyl-9-Dodecenoate was prepared as described in Step 1 of EXAMPLE 1.

Step 2: Cross-metathesis of methyl-9-dodecenoate with 1,4-dichloro-2-butene

Methyl 9-dodecenoate and 1,4-dichloro-2-butene were combined and degassed with argon for 30 minutes, then warmed to temperature (see, TABLE 5). Next, a metathesis catalyst (see, TABLE 5) was added to the methyl 9-dodecenoate and 1,4-dichloro-2-butene mixture. The mixture was then allowed to metathesize for the time reported in TABLE 5. GC analysis indicated that the product [CH₃O₂C(CH₂)₇CH═CHCH₂Cl] was produced in the GC yield reported in TABLE 5.

TABLE 5

Equiv of catalyst GC Area % Example 1,4-dichloro- loading Temp Product No. 2-butene catalyst (ppm) (° C.) 30 min 60 min 120 min 240 min 5-1 1 827 1000 60 ND ND ND 60.2 5-2 3 827 1000 60 ND ND ND 40.4 5-3 5 827 1000 60 ND ND ND 31.1 5-4² 2 827 1000 25 5.6 5.8 6.0 6.2 (60) 5-5¹ 2 827 500 25 34.6  34.5  35.0  35.1 (60) 5-6¹ 2 827 250 25 8.0 8.1 8.0 8.1 (60) 5-7¹ 2 827 100 25 1.6 1.5 1.6 1.6 (60) 5-8¹ 2 827 50 25 0.0 0.2 0.2 0.2 (60) * ND = no data ¹827 was initiated at 60° C., then reaction removed from heat to stir at room temp. Freshly distilled 1,4-dichloro-2-butene was used. ²1,4-dichloro-2-butene used directly from bottle with no distillation.

Example 6 Preparation of Methyl 12-Acetoxy-9-Dodecenoate from Methyl-9-dodecenoate and 3-Buten-1-yl Acetate

Step 1: Methyl 9-dodecenoate was prepared as described in Step 1 of EXAMPLE 1.

Step 2: Cross-Metathesis of methyl 9-dodecenoate with 3-buten-1-yl acetate.

Methyl 9-dodecenoate and 3-buten-1-yl acetate were combined and degassed with argon for 30 minutes, then warmed to temperature (see, TABLE 6). Next, a metathesis catalyst (see, TABLE 6) was added to the methyl 9-dodecenoate and 3-buten-1-yl acetate mixture. The mixture was then allowed to metathesize for the time reported in TABLE 6. GC analysis indicated that the product [CH₃O₂C(CH₂)₇CH═CH(CH₂)₂CO₂CH₃] was produced in the GC yield reported in TABLE 6.

TABLE 6

Equiv of catalyst GC Area % Example 3-buten-1-yl loading Temp Product No. acetate catalyst (ppm) (° C.) 30 min 60 min 120 min 240 min 6-1¹ 3 827 500 25 34.5 34.2 34.1 34.4 (60) 6-2 3 827 500 60 25.9 33.4 33.4 33.3 6-3 3 827 250 60 16.2 16.1 16.0 15.8 6-4 3 827 100 60 4.6 4.6 4.6 4.7 6-5 3 827 50 60 0.9 1.1 1.2 1.2 6-6 3 827 25 60 1.0 1.1 1.1 1.1 ¹827 was initiated at 60° C., then reaction removed from heat to stir at room temp.

Example 7 Preparation of Methyl 12-Trimethylsiloxy-9-Dodecenoate from Methyl 9-Dodecenoate and 3-Buten-1-yl trimethylsilyl ether

Step 1: Methyl 9-dodecenoate was prepared as described in Step 1 of EXAMPLE 1.

Step 2: Cross-Metathesis of Methyl 9-dodecenoate with 3-buten-1-yl trimethylsilyl ether.

Methyl 9-dodecenoate and 3-buten-1-yl trimethylsilyl ether were combined and degassed with argon for 30 minutes, then warmed to temperature (see, TABLE 7). Next, a metathesis catalyst (see, TABLE 7) was added to the methyl 9-dodecenoate and 3-buten-1-yl trimethylsilyl ether mixture. The mixture was then allowed to metathesize for the time reported in TABLE 7. GC analysis indicated that the product [CH₃O₂C(CH₂)₇CH═CH(CH₂)₂OSi(CH₃)₃] was produced in the GC yield reported in TABLE 7.

TABLE 7

Equiv of 3- buten-1-yl catalyst GC Area % Example trimethylsilyl loading Temp Product No. ether catalyst (ppm) (° C.) 30 min 60 min 120 min 240 min 7-1¹ 3 827 500 25 19.8 20.6 20.9 21.0 (60) 7-2 3 827 500 60 17.9 17.9 18.1 15.8 7-3 3 827 250 60 7.5 8.0 8.0 8.1 7-4 3 827 100 60 2.3 2.6 2.6 2.6 7-5 3 827 50 60 0.0 0.8 0.7 0.5 7-6 3 827 25 60 0.6 0.6 0.0 0.0 ¹827 was initiated at 60° C., then reaction removed from heat to stir at room temp.

Example 8 Preparation of Methyl 12-bromo-9-Dodecenoate from Methyl-9-dodecenoate and 1-bromo-3-hexene

Step 1: Methyl 9-dodecenoate was prepared as described in Step 1 of EXAMPLE 1.

Step 2: Cross-Metathesis of Methyl 9-dodecenoate with 1-bromo-3-hexene.

Methyl 9-dodecenoate and 1-bromo-3-hexene were combined and degassed with argon for 30 minutes, then warmed to temperature (see, TABLE 8). Next, a metathesis catalyst (see, TABLE 8) was added to the methyl 9-dodecenoate and 1-bromo-3-hexene mixture. The mixture was then allowed to metathesize for the time reported in TABLE 8. GC analysis indicated that the product [CH₃O₂C(CH₂)₇CH═CH(CH₂)₂Br] was produced in the GC yield reported in TABLE 8.

TABLE 8

Equiv of catalyst GC Area % Example 1-bromo- loading Temp Product No. 3-hexene catalyst (ppm) (° C.) 30 min 60 min 120 min 240 min 8-1 3 627 500 35 11.2 11.8 12.1 12.4 8-2 3 627 250 35 6.0 6.2 6.4 6.5 8-3 3 627 100 35 1.3 1.4 1.4 1.4

Example 9 Preparation of Methyl 11-chloro-9-undecenoate from Methyl-9-dodecenoate and allyl chloride

Step 1: Methyl 9-dodecenoate was prepared as described in Step 1 of EXAMPLE 1.

Step 2: Cross-Metathesis of methyl 9-dodecenoate with Allyl chloride.

Methyl 9-dodecenoate and allyl chloride were combined and degassed with argon for 30 minutes, then warmed to temperature (see, TABLE 9). Next, a metathesis catalyst (see, TABLE 9) was added to the methyl 9-dodecenoate and allyl chloride mixture. The mixture was then allowed to metathesize for the time reported in TABLE 9. GC analysis indicated that the product [CH₃O₂C(CH₂)₇CH═CHCH₂Cl] was produced in the GC yield reported in TABLE 9.

TABLE 9

catalyst GC Area % Example Equiv of loading Temp Product No. allyl chloride catalyst (ppm) (° C.) 30 min 60 min 120 min 240 min 9-1 3 627 500 35 15.6 15.3 14.9 15.1 9-2 3 627 250 35 5.1 5.4 5.4 5.1 9-3 3 627 100 35 0.9 1.0 0.9 0.8 9-4* 3 627 500 35 12.3 12.7 12.7 13.1 9-5* 3 627 250 35 9.9 10.4 10.3 10.7 9-6* 3 627 100 35 2.7 2.9 2.9 3.0 *Allyl chloride was freshly distilled.

Example 10 Preparation of Methyl 12,12-Diethoxy-9-Dodecenoate from Methyl-9-dodecenoate and 3-butenal diethyl acetal

Step 1: Methyl 9-dodecenoate was prepared as described in Step 1 of EXAMPLE 1.

Cross-Metathesis of methyl-9-dedecenoate with 3-butenal diethyl acetal.

Methyl 9-dodecenoate and 3-butenal diethyl acetal were combined and degassed with argon for 30 minutes, then warmed to temperature (see, TABLE 10). Next, a metathesis catalyst (see, TABLE 10) was added to the methyl 9-dodecenoate and 3-butenal diethyl acetal mixture. The mixture was then allowed to metathesize for the time reported in TABLE 10. GC analysis indicated that the product [CH₃O₂C(CH₂)₇CH═CHCH₂CH(OCH₂CH₃)₂] was produced in the GC yield reported in TABLE 10.

TABLE 10

Equiv of catalyst GC Area % 3-butenal loading Temp Product Exp # diethyl acetal Catalyst (ppm) (° C.) 30 min 60 min 120 min 240 min 10-1 3 827 500 60 6.6 7.2 7.5 7.3 10-2 3 827 250 60 3.0 3.5 3.6 3.5 10-3 3 827 100 60 1.0 1.2 1.3 1.2

Example 11 Preparation of Methyl 12-tert-Butoxy-9-Dodecenoate from Methyl-9-dodecenoate and 1-tert-butoxybut-3-ene

Step 1: Methyl 9-dodecenoate was prepared as described in Step 1 of EXAMPLE 1.

Step 2: Cross-Metathesis of methyl-9-dodecenoate with 1-tert-butoxybut-3-ene.

Methyl 9-dodecenoate and 1-tert-butoxybut-3-ene were combined and degassed with argon for 30 minutes, then warmed to temperature (see, TABLE 11). Next, a metathesis catalyst (see, TABLE 11) was added to the methyl 9-dodecenoate and 1-tert-butoxybut-3-ene mixture. The mixture was then allowed to metathesize for the time reported in TABLE 11. GC analysis indicated that the product [CH₃O₂C(CH₂)₇CH═CH(CH₂)₂OC(CH₃)₃] was produced in the GC yield reported in TABLE 11.

TABLE 11

Equiv of catalyst 1-tert-butoxy loading Temp GC Area % (Product) Exp # but-3-ene catalyst (ppm) (° C.) 30 min 60 min 120 min 240 min 11-1 3 827 1000 60 17.7 16.4 16.9 17.2 11-2 3 827 500 60 19.0 18.7 18.9 19.3 11-3 3 827 250 60 18.5 18.1 18.2 18.4

Other embodiments of this invention will be apparent to those skilled in the art upon consideration of this specification or from practice of the invention disclosed herein. Various omissions, modifications, and changes to the principles and embodiments described herein may be made by one skilled in the art without departing from the true scope and spirit of the invention which is indicated by the following claims. All patents, patent documents, and publications cited herein are hereby incorporated by reference as if individually incorporated. 

What is claimed is:
 1. A method of making a dicarboxylic acid alkene, dicarboxylate ester alkene, or dicarboxylate salt alkene, the method comprising the steps of: (a) providing a starting composition comprising one or more unsaturated fatty acids, unsaturated fatty esters, or unsaturated fatty acid salts, which comprise a residue selected from the group consisting of —C(O)—(CH2)7CH═CH—(CH2)7-CH3, —C(O)—(CH2)7CH═CH—CH2-CH═CH—(CH2)4-CH3, and —C(O)—(CH2)7CH═CH—CH2-CH═CH—CH2-CH═CH—CH2-CH3; (b) cross-metathesizing the composition of step (a) with 1-butene in the presence of a first metathesis catalyst, to form cross-metathesis products comprising: (i) one or more olefins having a terminal carbon-carbon double bond; and (ii) one or more acid-, ester-, or carboxylate salt-functionalized alkenes comprising a —C(O)—(CH2)7-CH═CH—CH2-CH3 residue; (c) separating at least a portion of one or more of the acid-, ester-, or carboxylate salt-functionalized alkenes of step (b) from the one or more olefins of step (b); and (d) self-metathesizing the separated acid-, ester-, or carboxylate salt-functionalized alkenes of step (c) in the presence of a second metathesis catalyst to form a composition comprising: (i) one or more dicarboxylic acid alkenes, dicarboxylate ester alkenes, or dicarboxylate salt alkenes, which comprise a —C(O)—(CH2)7-CH═CH—(CH2)7-C(O)— residue, and (ii) 3-hexene; wherein the first metathesis catalyst is a 2nd Generation Grubbs-type catalyst having the structure of formula (V):

wherein: M is a Group 8 transition metal; L² and L³ are independently neutral electron donor ligands; n is 0 or 1; m is 0, 1, or 2; X¹ and X² are independently anionic ligands; R¹ and R² are independently selected from hydrogen, hydrocarbyl, substituted hydrocarbyl, heteroatom-containing hydrocarbyl, substituted heteroatom-containing hydrocarbyl, and functional groups; X and Y are independently heteroatoms selected from N, O, S, and P; p and q are independently 0 or 1; Q¹, Q², Q³, and Q⁴ are independently linkers selected from the group consisting of hydrocarbylenes and substituted heteroatom-containing hydrocarbylenes; w, x, y, and z are independently zero or 1; and R³, R^(3A), R⁴, and R^(4A) are independently selected from hydrogen, hydrocarbyl, substituted hydrocarbyl, heteroatom-containing hydrocarbyl, and substituted heteroatom-containing hydrocarbyl.
 2. The method of claim 1, wherein the starting composition comprises an unsaturated polyol ester.
 3. The method of claim 2, wherein the starting composition is an unsaturated glyceride.
 4. The method of claim 1, wherein the starting composition is selected from the group consisting of: soybean oil, rapeseed oil, corn oil, sesame oil, cottonseed oil, sunflower oil, canola oil, safflower oil, palm oil, palm kernel oil, linseed oil, castor oil, olive oil, peanut oil, algae oil, tall oil, fish oil, lard, tallow, and combinations thereof.
 5. The method of claim 1, wherein the first and second metathesis catalysts are the same or different and selected from the group consisting of:

where Ph is phenyl, Mes is mesityl, py is pyridine, and Cy is cyclohexyl.
 6. The method of claim 1, wherein the first metathesis catalyst and the second metathesis catalyst are ruthenium-based metathesis catalysts.
 7. The method of claim 1, further comprising the step of hydrogenating the composition of step (d).
 8. The method of claim 1, further comprising the step of hydrolyzing an ester group of the dicarboxylate ester alkene to form a carboxylic acid group.
 9. A method of making a C18 dicarboxylic acid alkene, a C18 dicarboxylate ester alkene, a C18 dicarboxylate salt alkene, or a mixture thereof, the method comprising the steps of: (a) providing a composition comprising a Δ9 unsaturated fatty acid, a Δ9 unsaturated fatty ester, a Δ9 unsaturated fatty acid salt, or a mixture thereof; (b) cross-metathesizing the composition of step (a) with 1-butene in the presence of a first metathesis catalyst to form cross-metathesis products comprising (i) an acid-, ester-, or salt-functionalized alkene comprising a —C(O)—(CH₂)₇—CH═CH—CH₂—CH₃ residue; and (ii) an olefin having a terminal carbon-carbon double bond; (c) separating at least a portion of the acid-, ester-, or salt-functionalized olefin of step (b) from the olefin of step (b); and (d) self-metathesizing the separated acid-, ester-, or salt-functionalized olefin of step (c) in the presence of a second metathesis catalyst to form a composition comprising: (i) a C18 dicarboxylic acid alkene, a C18 dicarboxylate ester alkene, a C18 dicarboxylate salt alkene, or a mixture thereof, and (ii) 3-hexene, wherein the first metathesis catalyst is a 2nd Generation Grubbs-type catalyst having the structure of formula (V):

wherein: M is a Group 8 transition metal; L² and L³ are independently neutral electron donor ligands; n is 0 or 1; m is 0, 1, or 2; X¹ and X² are independently anionic ligands; R¹ and R² are independently selected from hydrogen, hydrocarbyl, substituted hydrocarbyl, heteroatom-containing hydrocarbyl, substituted heteroatom-containing hydrocarbyl, and functional groups; X and Y are independently heteroatoms selected from N, O, S, and P; p and q are independently 0 or 1; Q¹, Q², Q³, and Q⁴ are independently linkers selected from the group consisting of hydrocarbylenes and substituted heteroatom-containing hydrocarbylenes; w, x, y, and z are independently zero or 1; and R³, R^(3A), R⁴, and R^(4A) are independently selected from hydrogen, hydrocarbyl, substituted hydrocarbyl, heteroatom-containing hydrocarbyl, and substituted heteroatom-containing hydrocarbyl.
 10. The method of claim 9, further including the step of: (e) hydrogenating the composition of step (d) to form a saturated C18 dicarboxylic acid, saturated C18 dicarboxylate ester, saturated C18 dicarboxylate salt, or mixture thereof. 